A clean inspection outcome is typically seen as a positive regulatory signal for pharmaceutical manufacturers, particularly ...
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Zydus Lifesciences in focus after USFDA clears Ahmedabad plant, aflibercept biosimilar launch
Zydus Lifesciences is in focus after receiving USFDA clearance with zero observations for its Ahmedabad facility and ...
Alembic Pharmaceuticals completed a USFDA cGMP inspection at its Karakhadi Injectable Facility (F-3) from February 9–18, 2026. The inspection ended with two observations, none related to data ...
Currently, oral phenylephrine is widely used as a nasal decongestant active ingredient. (Image Credits: Pixabay) The U.S. Food and D rug Administration (USFDA) on Friday announced that it is proposing ...
Ahmedabad: Zydus Lifesciences Limited has secured final approval from the United States Food and Drug Administration (USFDA) for Bosentan tablets for oral suspension, 32 mg, further ...
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Aurobindo Pharma shares fall after USFDA flags severe contamination, data integrity failures
The USFDA further highlighted deficiencies in environmental monitoring in manufacturing areas, indicating gaps in ensuring controlled production conditions.
At current levels, the stock is trading about 6.8 percent below its 52-week high and nearly 19.79 percent above its 52-week ...
New Delhi: Alembic Pharmaceuticals on Thursday said it has received approval from the US health regulator to market a generic medication for seizures. The company has received approval from the US ...
Mumbai: Shares of Alembic Pharmaceuticals surged 13.61 percent on Monday after a major regulatory approval. The stock hit a high of Rs 1,104.10 during the day. The reason for this rise? Alembic got ...
The US Food and Drug Administration (USFDA) conducted an inspection of the company's Digwal (Telangana ) based plant from ...
Shares of Wockhardt Ltd soared 20 per cent in Monday's trade to hit a high of Rs 1,480.25 after the pharma company announced that the United States Food and Drug Administration (USFDA) has formally ...
New Delhi, Jan 2 : Drug firm Lupin has received final approval from the US health regulator to market cevimeline hydrochloride capsules, used for treatment of symptoms of dry mouth in patients with ...
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