5 Minutes Read

Confused about the term ‘soy milk’? FDA wants to know

KV Prasad Jun 13, 2022, 06:35 AM IST (Published)

 Listen to the Article (6 Minutes)

Summary

The call for comments, being published Thursday , comes after FDA Commissioner Scott Gottlieb signaled in July the agency might start going after non-dairy drinks that call themselves milk

Do people understand the differences between milk and soy and rice “milk”?

That’s what the Food and Drug Administration is asking as it considers whether soy and other non-dairy products can keep calling themselves “milk.” Right now, federal standards define milk as coming from a cow.

The call for comments, being published Thursday , comes after FDA Commissioner Scott Gottlieb signaled in July the agency might start going after non-dairy drinks that call themselves milk. The dairy industry for years has called for just such a crackdown.

Milk is one of a range of foods that have federal standards, which are supposed to ensure the quality of products on supermarket shelves.

Some makers of plant-based drinks say the standards are outdated and are used to fend off competition.

Elon Musk forms several ‘X Holdings’ companies to fund potential Twitter buyout

3 Mins Read

Thursday’s filing dispelled some doubts, though Musk still has work to do. He and his advisers will spend the coming days vetting potential investors for the equity portion of his offer, according to people familiar with the matter

 Daily Newsletter

KV Prasad Journo follow politics, process in Parliament and US Congress. Former Congressional APSA-Fulbright Fellow

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today's market

index Price Change
nifty 50 ₹16,986.00 -72.15
sensex ₹1,882.60 +28.30
nifty IT ₹2,206.80 +30.85
nifty bank ₹1,318.95 -14.95
index Price Change
nifty 50 ₹16,986.00 -7.15
sensex ₹1,882.60 +8.30
nifty IT ₹2,206.80 +3.85
nifty bank ₹1,318.95 -1.95
index Price Change
nifty 50 ₹16,986.00 -72.15
sensex ₹1,882.60 +28.30
nifty IT ₹2,206.80 +30.85
nifty bank ₹1,318.95 -14.95
index Price Change
nifty 50 ₹16,986.00 -7.15
sensex ₹1,882.60 +8.30
nifty IT ₹2,206.80 +3.85
nifty bank ₹1,318.95 -1.95
index Price Change
nifty 50 ₹16,986.00 -7.15
sensex ₹1,882.60 +8.30
nifty IT ₹2,206.80 +3.85
nifty bank ₹1,318.95 -1.95

Currency

Company Price Chng %Chng
Dollar-Rupee 73.3500 0.0000 0.00
Euro-Rupee 89.0980 0.0100 0.01
Pound-Rupee 103.6360 -0.0750 -0.07
Rupee-100 Yen 0.6734 -0.0003 -0.05
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 5 Minutes Read

Why the street is positive on Divi’s Labs

KV Prasad Jun 13, 2022, 06:35 AM IST (Published)

 Listen to the Article (6 Minutes)

Summary

Hyderabad-based Divi’s Labs is around a fresh 52 week high. In fact, the stock has outperformed most of its pharma peers in 2018, gaining 25 percent versus the Nifty Pharma index up 5 to 6 percent. And it seems the street expects the outperformance to continue.

Hyderabad-based Divi’s Labs is around a fresh 52 week high. In fact, the stock has outperformed most of its pharma peers in 2018, gaining 25 percent versus the Nifty Pharma index up 5 to 6 percent. And it seems the street expects the outperformance to continue.

For example, brokerage Phillip Capital in its latest note upgraded its rating on the stock to a ‘Buy; call hiking its target price to Rs 1,550 with an FY20E EPS hike of 5 percent. However, while prospects for Divi’s Labs seem to be bright now, one would have not thought the same in December 2016 or through most of 2017.

A Quick Recap

In December 7, 2016, Divi’s Labs informed the exchanges about an inspection at the company’s main unit located at Vishakapatnam, their Unit 2 facility.

The US Food and Drug Administration (FDA) had issued five observations to the plant. Five observations didn’t seem much especially for a company such as Divi’s that had a largely unblemished record, when it came to regulatory issues.

This confidence reflected in the stock, which held on to levels of around 1100 for the next few days. But this resilience only lasted till the details of the observations surfaced.

On December 23, 2016, the stock in one swoop corrected to close at 861, a 22 percent correction in one day and a 25 percent correction from the time the news of the inspection surfaced i.e. on the December 7.

The street feared the observations, which included lack of proper controls and inaccurate falsified documentation. The news worsened as Divi’s got slapped with an import alert three months later.

As expected, the correction extended with Divi’s falling below Rs 550 by May 2017. That meant an over 50 percent correction from the pre-USFDA inspection levels in December 2016.

Investors And Analysts Were Worried

Unit 2 was Divi’s Labs main facility shipping to the US. Fears of a prolonged regulatory issue such as those seen with Ranbaxy or Wockhardt loomed. That combined with the risk of other regulators taking cue from the FDA and an inspection still pending at their only other plant – Unit 1 also remained.

But, that was not to be. Divi’s Labs seemed to in fact set an example of a quick and efficient resolution. The green shoots seemed to emerge a few weeks after receiving the import alert in March itself.

The FDA exempted a few products from the facility. This fresh set of exempted products was in addition to 10 that were exempted earlier. That meant Divi’s Labs could continue manufacturing and supplying these products to the US, albeit probably with more regulations.

In July, the FDA lifted the 99-32, one of the two clauses under which an import alert was issued.

In July-August 2017, Unit 2 was also inspected by Irish and Slovenian regulators. The inspection was a general inspection, which was successful with no critical observations. This was another confidence boost for Divi’s.

However, the biggest surprise of them all was a USFDA re-inspection of the Unit 2 facility in September 2017, less than a year of an import alert being issued.

The FDA was satisfied with the company’s remediation. The import alert was lifted in November 2017 and was moving to close the warning letter issued to Unit 2.

Unprecedented and Unbelievable

Divi’s Labs managed to solve an import alert on its main facility in less than a year. Yes, this resolution might have been a one off case, but Divi’s Labs was out of the woods. This confidence reflected in the stock. The stock rallied back to its pre-regulatory issues levels of 1,100 by Jan 2018 and has now extended the rally to over 1,300.

One of the reasons for this confidence on the stock is probably the company re-earning its past reputation of good compliance.

Besides resolving the import alert, Divi’s, for example, solved six fresh observations issued to Unit 2 facility, which was issued in September 2017. Divi’s managed to remediate the problems and received an Establishment Inspection Report for the facility in November 2017.

Unit 2 also got the green light from the Japanese and Australian authorities in October and November 2017. The risk from a Unit 1 plant inspection also doesn’t remain. The USFDA inspected Unit 1 in May 2018 with no observations, giving the unit a go ahead.

Earnings Recovery

FY18 was a washout year for Divi’s Labs. Earnings were impacted due to the import alert and subsequent remediation at its Unit 2 facility.

The company ended FY18 with revenue falling 6 percent to Rs 3,837 crore, EBITDA (Earnings before interest, taxes, depreciation, and amortisation) falling 13 percent, margins correcting to 32.6 percent against 35.4 percent in FY17 and profit falling 17 percent to around Rs 870 crore.

But the street is confident about the future and believe earnings should pick up. Q1 for example, was a quarter of normalised operations, i.e. not impacted by ongoing remediation or audits by the US FDA.

In Q1FY19, the company recorded a revenue growth of 21 percent to Rs 955 crore, EBITDA spiking 44 percent to Rs 352 crore and margins recovering to 35 percent against 30 percent in Q1FY18 with a profit of Rs 266 crore. The earnings per share (EPS) for Q1FY19 itself was Rs 10 against Rs 6.65 a year ago and Rs 32 for the whole of FY18.

Confident Despite Customer Consolidation

Divi’s Labs generated around 60-70 percent of its sales from regulated markets, US and Europe. Despite price pressure and vendor consolidation impacting US market, the company says it’s confident.

Divi’s Labs believes that the company plays a ‘complementary’ and ‘non conflicting’ role with their customers. And their product portfolio combined with the long standing relationships with customers, make them the vendor of choice.

Lastly, analysts believe the API (active pharmaceutical ingredient) supply disruption in China will also be an opportunity for Divi’s. Currently, China is the lead supplier of APIs globally and in India. China supplies 20 percent API’s globally and 70-80 percent of India’s requirements.

However, many Chinese suppliers are shutting capacities due to environmental concerns. This has resulted in supply-chain problems, shortages of some APIs and a consequent spikes in prices.

Analysts expect these supply disruptions to be a multiyear opportunity for Divis. Analysts believe this is when the company can leverage its long term partnerships to remain a supplier of choice and acquire new clients.

Divi’s is currently looking at alternatives to ensure continuing supply. Besides that, they are evaluating backward integration for starting materials.

Divi’s is also looking at capex to take advantage of the opportunities. They believe there are some patents of products, which could be expiring soon.

The to capitalise on these opportunities, the company is investing Rs 400 crore in a brownfield expansion at its SEZ in Vishakapatnam. Analysts also expect the company’s Rs 700 crore Kakinada greenfield plant that has been stuck with environmental and land hurdles getting the go ahead soon.

Elon Musk forms several ‘X Holdings’ companies to fund potential Twitter buyout

3 Mins Read

Thursday’s filing dispelled some doubts, though Musk still has work to do. He and his advisers will spend the coming days vetting potential investors for the equity portion of his offer, according to people familiar with the matter

 Daily Newsletter

KV Prasad Journo follow politics, process in Parliament and US Congress. Former Congressional APSA-Fulbright Fellow

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Oil Fluctuates as Traders Assess China’s Vow, Unrest in Libya

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index Price Change
nifty 50 ₹16,986.00 -72.15
sensex ₹1,882.60 +28.30
nifty IT ₹2,206.80 +30.85
nifty bank ₹1,318.95 -14.95
index Price Change
nifty 50 ₹16,986.00 -7.15
sensex ₹1,882.60 +8.30
nifty IT ₹2,206.80 +3.85
nifty bank ₹1,318.95 -1.95
index Price Change
nifty 50 ₹16,986.00 -72.15
sensex ₹1,882.60 +28.30
nifty IT ₹2,206.80 +30.85
nifty bank ₹1,318.95 -14.95
index Price Change
nifty 50 ₹16,986.00 -7.15
sensex ₹1,882.60 +8.30
nifty IT ₹2,206.80 +3.85
nifty bank ₹1,318.95 -1.95
index Price Change
nifty 50 ₹16,986.00 -7.15
sensex ₹1,882.60 +8.30
nifty IT ₹2,206.80 +3.85
nifty bank ₹1,318.95 -1.95

Currency

Company Price Chng %Chng
Dollar-Rupee 73.3500 0.0000 0.00
Euro-Rupee 89.0980 0.0100 0.01
Pound-Rupee 103.6360 -0.0750 -0.07
Rupee-100 Yen 0.6734 -0.0003 -0.05
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 5 Minutes Read

US arm of Intas Pharma recalls over 46,000 bottles of tablets

KV Prasad Jun 13, 2022, 06:35 AM IST (Published)

 Listen to the Article (6 Minutes)

Summary

Hydrochlorothiazide tablets belong to a class of drugs known as diuretics and are used for treatment of high blood pressure and edema.

Accord Healthcare Inc, the US arm of Intas Pharmaceuticals, is recalling over 46,000 bottles of Hydrochlorothiazide tablets manufactured by the Ahmedabad-based firm, on account of labelling mix-up, USFDA said.

Hydrochlorothiazide tablets belong to a class of drugs known as diuretics and are used for treatment of high blood pressure and edema.

Accord Healthcare is recalling 46,632 bottles of Hydrochlorothiazide tablets USP in the strength of 12.5 mg, the Enforcement Report by United States Food and Drug Administration (USFDA) said.

The reason for the recall is “Labelling: label mix-up: customer complaint that a sealed bottle labelled as Hydrochlorothiazide tablets USP 12.5 mg contained only Spironolactone tablets USP 25 mg,” it added.

The voluntary nationwide recall in the US and Puerto Rico has not been classified yet, the report said.

Elon Musk forms several ‘X Holdings’ companies to fund potential Twitter buyout

3 Mins Read

Thursday’s filing dispelled some doubts, though Musk still has work to do. He and his advisers will spend the coming days vetting potential investors for the equity portion of his offer, according to people familiar with the matter

 Daily Newsletter

KV Prasad Journo follow politics, process in Parliament and US Congress. Former Congressional APSA-Fulbright Fellow

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Oil Fluctuates as Traders Assess China’s Vow, Unrest in Libya

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today's market

index Price Change
nifty 50 ₹16,986.00 -72.15
sensex ₹1,882.60 +28.30
nifty IT ₹2,206.80 +30.85
nifty bank ₹1,318.95 -14.95
index Price Change
nifty 50 ₹16,986.00 -7.15
sensex ₹1,882.60 +8.30
nifty IT ₹2,206.80 +3.85
nifty bank ₹1,318.95 -1.95
index Price Change
nifty 50 ₹16,986.00 -72.15
sensex ₹1,882.60 +28.30
nifty IT ₹2,206.80 +30.85
nifty bank ₹1,318.95 -14.95
index Price Change
nifty 50 ₹16,986.00 -7.15
sensex ₹1,882.60 +8.30
nifty IT ₹2,206.80 +3.85
nifty bank ₹1,318.95 -1.95
index Price Change
nifty 50 ₹16,986.00 -7.15
sensex ₹1,882.60 +8.30
nifty IT ₹2,206.80 +3.85
nifty bank ₹1,318.95 -1.95

Currency

Company Price Chng %Chng
Dollar-Rupee 73.3500 0.0000 0.00
Euro-Rupee 89.0980 0.0100 0.01
Pound-Rupee 103.6360 -0.0750 -0.07
Rupee-100 Yen 0.6734 -0.0003 -0.05
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 5 Minutes Read

Lupin gets USFDA nod to market Atovaquone oral suspension

KV Prasad Jun 13, 2022, 06:35 AM IST (Published)

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Summary

Drug firm Lupin Wednesday said it has received nod from the US health regulator to market its Atovaquone oral suspension used for prevention and treatment of a type of pneumonia.

Drug firm Lupin Wednesday said it has received nod from the US health regulator to market its Atovaquone oral suspension used for prevention and treatment of a type of pneumonia.

The company has received approval to market generic Atovaquone oral suspension USP in the strength of 750 mg/5 mL from the United States Food and Drug Administration (USFDA), Lupin said in a BSE filing.

The product is a generic version of GlaxoSmithKline LLC’s Mepron oral suspension in the same strength, it added.

As per IQVIA MAT June 2018 data, Atovaquone oral suspension, 750 mg/5 mL had annual sales of around USD 117.4 million in the US, Lupin said.

The product is “indicated for prevention and acute oral treatment of mild-to moderate pneumocystis carinii pneumonia (PCP) in patients intolerant to trimethoprim-sulfamethoxazole,” it added.

Shares of Lupin Ltd today closed at Rs 956.35 per scrip on BSE, up 1.78 per cent from its previous close.

Elon Musk forms several ‘X Holdings’ companies to fund potential Twitter buyout

3 Mins Read

Thursday’s filing dispelled some doubts, though Musk still has work to do. He and his advisers will spend the coming days vetting potential investors for the equity portion of his offer, according to people familiar with the matter

 Daily Newsletter

KV Prasad Journo follow politics, process in Parliament and US Congress. Former Congressional APSA-Fulbright Fellow

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Oil Fluctuates as Traders Assess China’s Vow, Unrest in Libya

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today's market

index Price Change
nifty 50 ₹16,986.00 -72.15
sensex ₹1,882.60 +28.30
nifty IT ₹2,206.80 +30.85
nifty bank ₹1,318.95 -14.95
index Price Change
nifty 50 ₹16,986.00 -7.15
sensex ₹1,882.60 +8.30
nifty IT ₹2,206.80 +3.85
nifty bank ₹1,318.95 -1.95
index Price Change
nifty 50 ₹16,986.00 -72.15
sensex ₹1,882.60 +28.30
nifty IT ₹2,206.80 +30.85
nifty bank ₹1,318.95 -14.95
index Price Change
nifty 50 ₹16,986.00 -7.15
sensex ₹1,882.60 +8.30
nifty IT ₹2,206.80 +3.85
nifty bank ₹1,318.95 -1.95
index Price Change
nifty 50 ₹16,986.00 -7.15
sensex ₹1,882.60 +8.30
nifty IT ₹2,206.80 +3.85
nifty bank ₹1,318.95 -1.95

Currency

Company Price Chng %Chng
Dollar-Rupee 73.3500 0.0000 0.00
Euro-Rupee 89.0980 0.0100 0.01
Pound-Rupee 103.6360 -0.0750 -0.07
Rupee-100 Yen 0.6734 -0.0003 -0.05
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Should Elon Musk be able to buy Twitter?

USFDA to inspect Sun Pharma’s Mohali unit today

SunPharma earnings

The US Food and Drug Administration (US FDA) is set to inspect Sun Pharma’s Mohali plant on Monday.

The Mohali unit was Ranbaxy’s unit which Sun Pharma acquired when they acquired Ranbaxy in 2015. The USFDA, sometime ago, had lifted the import alert some time ago on Mohali unit but sources told CNBC-TV18 that there will be a surprise inspection on Monday.

>>Sun Pharma in USFDA crosshairs, but market bullish on stock

Sun Pharma did not comment on likely USFDA inspection at Mohali.

 5 Minutes Read

Lupin gets USFDA nod for generic Potassium Chloride Oral Solution

KV Prasad Jun 13, 2022, 06:35 AM IST (Published)

 Listen to the Article (6 Minutes)

Summary

Drug firm, Lupin, on Friday said it has received approval from the US health regulator to sell its potassium chloride oral solution used for treatment of low potassium levels in the American market.

Drug firm, Lupin, on Friday said it has received approval from the US health regulator to sell its potassium chloride oral solution used for treatment of low potassium levels in the American market.

The company has received approval to market its Potassium chloride oral solution USP, in the strengths of 20 mEq/15 mL (10 per cent) and 40 mEq/15 mL (20 per cent) from the United States Food and Drug Administration (USFDA), Lupin said in a filing to BSE.

The company’s product is generic version of Genus Lifesciences Inc’s Potassium chloride oral solution in the same strengths, it added.

As per IQVIA MAT June 2018 data the oral solution in the two strengths had annual sales of around USD 184.95 million in the US, Lupin said.

“The product is indicated for the treatment and prophylaxis of hypokalemia with or without metabolic alkalosis, in patients for whom dietary management with potassium-rich foods and/or diuretic dose reduction are insufficient,” it added.

Shares of Lupin Ltd were trading at Rs 933.35 on BSE, up 4.44 percent from the previous close.

Elon Musk forms several ‘X Holdings’ companies to fund potential Twitter buyout

3 Mins Read

Thursday’s filing dispelled some doubts, though Musk still has work to do. He and his advisers will spend the coming days vetting potential investors for the equity portion of his offer, according to people familiar with the matter

 Daily Newsletter

KV Prasad Journo follow politics, process in Parliament and US Congress. Former Congressional APSA-Fulbright Fellow

Previous Article

Oil Fluctuates as Traders Assess China’s Vow, Unrest in Libya

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today's market

index Price Change
nifty 50 ₹16,986.00 -72.15
sensex ₹1,882.60 +28.30
nifty IT ₹2,206.80 +30.85
nifty bank ₹1,318.95 -14.95
index Price Change
nifty 50 ₹16,986.00 -7.15
sensex ₹1,882.60 +8.30
nifty IT ₹2,206.80 +3.85
nifty bank ₹1,318.95 -1.95
index Price Change
nifty 50 ₹16,986.00 -72.15
sensex ₹1,882.60 +28.30
nifty IT ₹2,206.80 +30.85
nifty bank ₹1,318.95 -14.95
index Price Change
nifty 50 ₹16,986.00 -7.15
sensex ₹1,882.60 +8.30
nifty IT ₹2,206.80 +3.85
nifty bank ₹1,318.95 -1.95
index Price Change
nifty 50 ₹16,986.00 -7.15
sensex ₹1,882.60 +8.30
nifty IT ₹2,206.80 +3.85
nifty bank ₹1,318.95 -1.95

Currency

Company Price Chng %Chng
Dollar-Rupee 73.3500 0.0000 0.00
Euro-Rupee 89.0980 0.0100 0.01
Pound-Rupee 103.6360 -0.0750 -0.07
Rupee-100 Yen 0.6734 -0.0003 -0.05
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Should Elon Musk be able to buy Twitter?

 5 Minutes Read

Drug firm Zydus Cadila gets USFDA nod for cholesterol, antipsychotic drugs

KV Prasad Jun 13, 2022, 06:35 AM IST (Published)

 Listen to the Article (6 Minutes)

Summary

The company has received USFDA’s final clearance to market Gemfibrozil tablets in strength of 600 mg and the other product in strengths of 10 mg, 15 mg, 20 mg, and 30 mg, Zydus Cadila said in a statement.

Drug firm Zydus Cadila today said it has received final approval from the US health regulator to market Gemfibrozil tablets and Aripiprazole orally disintegrating tablets in the US.

The company has received USFDA’s final clearance to market Gemfibrozil tablets in strength of 600 mg and the other product in strengths of 10 mg, 15 mg, 20 mg, and 30 mg, Zydus Cadila said in a statement.

“Both the drugs will be manufactured at the group’s formulations manufacturing facility at Moraiya, Ahmedabad,” it added.

Gemfibrozil tablets are used together with diet to treat very high cholesterol and triglyceride levels in people with pancreatitis, Zydus Cadila said.

The drug is also used to lower the risk of stroke, heart attack or other heart complications in people with high cholesterol and triglycerides who have not benefitted from other treatments, it added.

“Aripiprazole is an atypical antipsychotic. The drug is used to treat certain mental/mood disorders, such as bipolar disorder, schizophrenia, Tourette’s disorder, and irritability associated with autistic disorder,” Zydus Cadila said.

It may also be used in combination with other medication to treat depression, it added.

The group now has 215 approvals and has so far filed over 330 abbreviated new drug applications (ANDAs), Zydus Cadila said.

Shares of Cadila Healthcare, the listed entity of the group, were today trading at Rs 393 per scrip on BSE, up 1.62 percent from the previous close.

Elon Musk forms several ‘X Holdings’ companies to fund potential Twitter buyout

3 Mins Read

Thursday’s filing dispelled some doubts, though Musk still has work to do. He and his advisers will spend the coming days vetting potential investors for the equity portion of his offer, according to people familiar with the matter

 Daily Newsletter

KV Prasad Journo follow politics, process in Parliament and US Congress. Former Congressional APSA-Fulbright Fellow

Previous Article

Oil Fluctuates as Traders Assess China’s Vow, Unrest in Libya

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Shanghai residents turn to NFTs to record COVID lockdown, combat censorship

LIVE TV

today's market

index Price Change
nifty 50 ₹16,986.00 -72.15
sensex ₹1,882.60 +28.30
nifty IT ₹2,206.80 +30.85
nifty bank ₹1,318.95 -14.95
index Price Change
nifty 50 ₹16,986.00 -7.15
sensex ₹1,882.60 +8.30
nifty IT ₹2,206.80 +3.85
nifty bank ₹1,318.95 -1.95
index Price Change
nifty 50 ₹16,986.00 -72.15
sensex ₹1,882.60 +28.30
nifty IT ₹2,206.80 +30.85
nifty bank ₹1,318.95 -14.95
index Price Change
nifty 50 ₹16,986.00 -7.15
sensex ₹1,882.60 +8.30
nifty IT ₹2,206.80 +3.85
nifty bank ₹1,318.95 -1.95
index Price Change
nifty 50 ₹16,986.00 -7.15
sensex ₹1,882.60 +8.30
nifty IT ₹2,206.80 +3.85
nifty bank ₹1,318.95 -1.95

Currency

Company Price Chng %Chng
Dollar-Rupee 73.3500 0.0000 0.00
Euro-Rupee 89.0980 0.0100 0.01
Pound-Rupee 103.6360 -0.0750 -0.07
Rupee-100 Yen 0.6734 -0.0003 -0.05
Quiz
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Are you a Crypto Head? It’s time to prove it!
10 Questions · 5 Minutes
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What coins do you think will be valuable over next 3 years?

Answer Anonymously

Should Elon Musk be able to buy Twitter?

 5 Minutes Read

Zydus Cadila gets USFDA nod to market two products

KV Prasad Jun 13, 2022, 06:35 AM IST (Published)

 Listen to the Article (6 Minutes)

Summary

Drug firm Zydus Cadila on Thursday said it has received final approval from the US health regulator to market Gemfibrozil tablets and Aripiprazole orally disintegrating tablets in the US.

Drug firm Zydus Cadila on Thursday said it has received final approval from the US health regulator to market Gemfibrozil tablets and Aripiprazole orally disintegrating tablets in the US.

The company has received USFDA’s final clearance to market Gemfibrozil tablets in strength of 600 mg and the other product in strengths of 10 mg, 15 mg, 20 mg, and 30 mg, Zydus Cadila said in a statement.

“Both the drugs will be manufactured at the group’s formulations manufacturing facility at Moraiya, Ahmedabad,” it added.

Gemfibrozil tablets are used together with diet to treat very high cholesterol and triglyceride levels in people with pancreatitis, Zydus Cadila said.

The drug is also used to lower the risk of stroke, heart attack or other heart complications in people with high cholesterol and triglycerides who have not beneftted from other treatments, it added.

“Aripiprazole is an atypical antipsychotic. The drug is used to treat certain mental/mood disorders, such as bipolar disorder, schizophrenia, Tourette’s disorder, and irritability associated with autistic disorder,” Zydus Cadila said.

It may also be used in combination with other medication to treat depression, it added.

The group now has 215 approvals and has so far filed over 330 abbreviated new drug applications (ANDAs), Zydus Cadila said.

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KV Prasad Journo follow politics, process in Parliament and US Congress. Former Congressional APSA-Fulbright Fellow

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index Price Change
nifty 50 ₹16,986.00 -72.15
sensex ₹1,882.60 +28.30
nifty IT ₹2,206.80 +30.85
nifty bank ₹1,318.95 -14.95
index Price Change
nifty 50 ₹16,986.00 -7.15
sensex ₹1,882.60 +8.30
nifty IT ₹2,206.80 +3.85
nifty bank ₹1,318.95 -1.95
index Price Change
nifty 50 ₹16,986.00 -72.15
sensex ₹1,882.60 +28.30
nifty IT ₹2,206.80 +30.85
nifty bank ₹1,318.95 -14.95
index Price Change
nifty 50 ₹16,986.00 -7.15
sensex ₹1,882.60 +8.30
nifty IT ₹2,206.80 +3.85
nifty bank ₹1,318.95 -1.95
index Price Change
nifty 50 ₹16,986.00 -7.15
sensex ₹1,882.60 +8.30
nifty IT ₹2,206.80 +3.85
nifty bank ₹1,318.95 -1.95

Currency

Company Price Chng %Chng
Dollar-Rupee 73.3500 0.0000 0.00
Euro-Rupee 89.0980 0.0100 0.01
Pound-Rupee 103.6360 -0.0750 -0.07
Rupee-100 Yen 0.6734 -0.0003 -0.05
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 5 Minutes Read

Strides Pharma Science receives acceptance from USFDA for two ANDAs

KV Prasad Jun 13, 2022, 06:35 AM IST (Published)

 Listen to the Article (6 Minutes)

Summary

Strides Pharma Science on Wednesday said its step-down wholly owned subsidiary has received acceptance from the US health regulator for two key abbreviated new drug applications (ANDAs).

Strides Pharma Science on Wednesday said its step-down wholly owned subsidiary has received acceptance from the US health regulator for two key abbreviated new drug applications (ANDAs).

“Strides Pharma Global Pte. Ltd, Singapore, received ANDA ‘acceptable for filing’ correspondence from the US Food and Drug Administration (USFDA) for two key ANDAs that met the prioritisation factors as a potential first generic,” Strides Pharma Science said in a regulatory filing.

The company said the two products could be eligible for a potential 180-day exclusivity.

Quoting IQVIA MAT data, Strides Pharma Science said the US market for these products cumulatively is $550 million.

“The USFDA also granted Strides’ request to designate the drug product under these ANDAs as a competitive generic therapy (CGT),” it added.

Strides Pharma Science said approval of the CGT designated ANDAs will be contingent on certain conditions including continued USFDA approval status for the manufacturing plant, API supplier.

Elon Musk forms several ‘X Holdings’ companies to fund potential Twitter buyout

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Thursday’s filing dispelled some doubts, though Musk still has work to do. He and his advisers will spend the coming days vetting potential investors for the equity portion of his offer, according to people familiar with the matter

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KV Prasad Journo follow politics, process in Parliament and US Congress. Former Congressional APSA-Fulbright Fellow

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index Price Change
nifty 50 ₹16,986.00 -72.15
sensex ₹1,882.60 +28.30
nifty IT ₹2,206.80 +30.85
nifty bank ₹1,318.95 -14.95
index Price Change
nifty 50 ₹16,986.00 -7.15
sensex ₹1,882.60 +8.30
nifty IT ₹2,206.80 +3.85
nifty bank ₹1,318.95 -1.95
index Price Change
nifty 50 ₹16,986.00 -72.15
sensex ₹1,882.60 +28.30
nifty IT ₹2,206.80 +30.85
nifty bank ₹1,318.95 -14.95
index Price Change
nifty 50 ₹16,986.00 -7.15
sensex ₹1,882.60 +8.30
nifty IT ₹2,206.80 +3.85
nifty bank ₹1,318.95 -1.95
index Price Change
nifty 50 ₹16,986.00 -7.15
sensex ₹1,882.60 +8.30
nifty IT ₹2,206.80 +3.85
nifty bank ₹1,318.95 -1.95

Currency

Company Price Chng %Chng
Dollar-Rupee 73.3500 0.0000 0.00
Euro-Rupee 89.0980 0.0100 0.01
Pound-Rupee 103.6360 -0.0750 -0.07
Rupee-100 Yen 0.6734 -0.0003 -0.05
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Baxter gets USFDA warning letter on recently acquired Claris plant

KV Prasad Jun 13, 2022, 06:35 AM IST (Published)

 Listen to the Article (6 Minutes)

Summary

Baxter, in 2017 bought Gujarat-based Claris Injectables’ business for $625 million.

On July 5, 2018, US Food and Drug Administration (USFDA) issued a warning letter to American injectable manufacturer Baxter for violating current good manufacturing practice norms at its Gujarat plant.

Under normal circumstances, it would have been qualified as just another instance of a multinational pharma company facing issues at its Indian facility.

But the story for Baxter’s warning letter runs deeper. The warning letter was issued to what was Claris Injectables’ plant that Baxter acquired just a year ago.

It was the second warning letter issued to the same facility in the last eight years.

It was also the third time in the past decade that a pharma company  after buying an Indian pharma business.

The other two instances were Daiichy-Ranbaxy and Mylan-Agila.

A Brief On The Baxtar-Claris Deal

Baxter, in 2017 bought Gujarat-based Claris Injectables’ business for $625 million. It was the second big transaction in the Indian injectable space within the span of a few months.

The first was China’s Fosun buying 86 percent stake in Indian unlisted injectable manufacturer Gland Pharma for $1.3 billion. Eventually, it revised down to Fosun buying 74 percent stake for $1.1 billion.

This latest warning letter did not surprise experts. Based on Claris’s regulatory history, Baxter should have been more cautious.

In fact, the Ahmedabad injectable plant had five observations outstanding from the USFDA when the transaction was announced. And as luck would have it, the USFDA started a re-inspection of the facility in question on July 27, 2017, the same day Baxter-Claris announced the transaction.

The July 2017 inspection continued till the first week of August. It was conducted by USFDA inspectors Thomas Arista and Massoud Motamed.

In what was one of the highest number of observations received by an Indian plant in recent times (Sun Pharma’s Halol plant got 23 observations on September 14), the USFDA issued 18 observations on the Ahmedabad facility.

The seventeen-page Form 483 was addressed to Jacqueline Kunzler, the global head of quality of Baxter. At that time, Baxter had no control over quality systems. It was these 18 observations that converted into a warning letter that we are discussing now.

Experts wonder why Baxter didn’t exit the deal after the adverse observations.

In fact, during the post-deal conference call, Claris Life pointed out that a possible threshold for the deal between the two companies would be a possible escalation of the five USFDA observations issued in August 2016.

Maybe it was Baxter’s impatience to grow its global footprint coupled with the sting of losing Gland Pharma to Fosun and a confidence to solve regulatory issues that resulted in them staying on.

In any case, experts say Baxter should have read the signs in Claris’s regulatory history.

Following is a brief timeline on key regulatory issues faced by Claris in the past.

2010

In June and July 2010, Claris’s facility in Ahmedabad and the US facility located at New Jersey was inspected by the USFDA. These inspections saw an adverse outcome with the USFDA issuing a warning letter in November 2010, pointing out lapses in good manufacturing practices.

The warning letter pointed out instances of marketing an unapproved new drug without an approved application.

Violations included complaints of IV bags of containing fungus. The USFDA expressed their concern about inadequate investigations and process deviations.

It took Claris almost two years to solve the issues. In August 2012, the company said it had formally received a letter from the USFDA indicating that the outstanding issues were addressed.

2015

The USFDA inspection conducted from May 4 to 11, issued the Ahmedabad plant five observations. The observations included insufficient procedures, issues in sampling and deficiencies in training and design. A year later, in May 2016, the company received an Establishment Inspection Report.

2016

In August 2016, the USFDA re-inspected the Ahmedabad facility. The inspection lasted 10 days and was issued five observations. These observations included lack of production and process controls, issues with the quality control unit and procedures to prevent microbiological contamination not being followed, amongst others.

As mentioned earlier, these five observations issued in August 2016 were not closed by the time negotiations between Baxter-Claris reached final stages in June 2017.

Baxter-Claris announced the deal on July 27, 2017, and the same day the USFDA started their re-inspection of the Ahmedabad facility. The 18 observations issued in this inspection included issues on environmental monitoring, lack of documentation practices, out of specification results invalidated, water leakage, and false media fill records amongst others.

These 18 observations were escalated to a warning letter on July 5, 2018. In the warning letter addressed to Amish Vyas, managing director of Baxter, the USFDA pointed out significant violations.

It included lack of investigations into out of specification results, a ‘worrisome’ history of recalls citing examples in 2010 and 2017. Other issues included the operator recording unreliable data with lack of explanations from senior managers. The warning letter pointed out the need for the data integrity remediation. In November 2010, the USFDA cited lapses with repeat violations at the facility.

The positive for Baxter might be the fact that the USFDA is aware that Baxter acquired the facility the same the day inspection began and is seeking a meeting with Baxter management. But it is still expected to be a long road ahead for Baxter to solve these regulatory issues.

It could entail tough decisions such as starting operations from scratch including employing stringent measures of revamping machinery and personnel.

Besides another case of regulatory issues on an Indian facility, the larger takeaway is that this incident is another example of a red flag on the ‘India image’.

More on the two instances I mentioned at the start of this article of MNCs getting the short end of the stick post an Indian merger and acquisition.

In 2008, after Daiichi bought Ranbaxy for over Rs 20,000 crore, the company in the same year was lapped with import alerts on Ranbaxy plant in Paonta Sahib, Dewas. By the time Daiichi sold Ranbaxy to Sun Pharma in 2015, it had entered into a consent decree on its key plants with the USFDA, pleaded guilty to charges of improper manufacturing charges and settled on a record $500 million fine.

In 2013, Mylan bought Stride’s injectable business Agila for $1.75 billion. In 2015, Mylan soon got slapped with a warning letter for the injectable plants acquired from Strides. Mylan apparently overhauled systems to the extent of firing old and hiring new personnel who could be trained to avoid quality lapses.

The entire process of Mylan-Agila saga indicates that the company was more vigilant about the deals in India. It wouldn’t be a surprise if other MNCs including Baxter think the same.

Elon Musk forms several ‘X Holdings’ companies to fund potential Twitter buyout

3 Mins Read

Thursday’s filing dispelled some doubts, though Musk still has work to do. He and his advisers will spend the coming days vetting potential investors for the equity portion of his offer, according to people familiar with the matter

 Daily Newsletter

KV Prasad Journo follow politics, process in Parliament and US Congress. Former Congressional APSA-Fulbright Fellow

Previous Article

Oil Fluctuates as Traders Assess China’s Vow, Unrest in Libya

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Shanghai residents turn to NFTs to record COVID lockdown, combat censorship

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today's market

index Price Change
nifty 50 ₹16,986.00 -72.15
sensex ₹1,882.60 +28.30
nifty IT ₹2,206.80 +30.85
nifty bank ₹1,318.95 -14.95
index Price Change
nifty 50 ₹16,986.00 -7.15
sensex ₹1,882.60 +8.30
nifty IT ₹2,206.80 +3.85
nifty bank ₹1,318.95 -1.95
index Price Change
nifty 50 ₹16,986.00 -72.15
sensex ₹1,882.60 +28.30
nifty IT ₹2,206.80 +30.85
nifty bank ₹1,318.95 -14.95
index Price Change
nifty 50 ₹16,986.00 -7.15
sensex ₹1,882.60 +8.30
nifty IT ₹2,206.80 +3.85
nifty bank ₹1,318.95 -1.95
index Price Change
nifty 50 ₹16,986.00 -7.15
sensex ₹1,882.60 +8.30
nifty IT ₹2,206.80 +3.85
nifty bank ₹1,318.95 -1.95

Currency

Company Price Chng %Chng
Dollar-Rupee 73.3500 0.0000 0.00
Euro-Rupee 89.0980 0.0100 0.01
Pound-Rupee 103.6360 -0.0750 -0.07
Rupee-100 Yen 0.6734 -0.0003 -0.05
Quiz
Powered by
Are you a Crypto Head? It’s time to prove it!
10 Questions · 5 Minutes
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Win WRX (WazirX token) worth Rs. 1500.
Question 1 of 5

What coins do you think will be valuable over next 3 years?

Answer Anonymously

Should Elon Musk be able to buy Twitter?