Granules Pharmaceuticals clears US FDA audit
The company had undergone the PAI audit by the US Food and Drug Administration (FDA) from 21st June, 2021 to 25th June, 2021.
July 23, 2021
by expresspharma
Granules pledges 16 crore Paracetamol tablets to Telangana government to fight COVID-19
The company will provide one crore tablets every week, starting from today 12th May 2021, aggregating to 16 crore tablets worth Rs 8 crores over next four months.
May 14, 2021
by expresspharma
Granules India gets USFDA approval for OTC Acetaminophen, Aspirin and Caffeine Tablets
Granules India announced that the US Food & Drug Administration (US FDA) has approved its Abbreviated New Drug Application (ANDA) for Acetaminophen, Aspirin and Caffeine Tablets USP, 250 mg/250 mg/65 mg (OTC).
February 25, 2021
by expresspharma
Granules India gets US FDA approval for Potassium Chloride ER Capsules
Potassium Chloride is indicated for the treatment of patients with hypokalemia with or without metabolic alkalosis, in digitalis intoxications, and in patients with hypokalemic familial periodic paralysis.
February 18, 2021
by expresspharma
Granules India gets US FDA nod for Potassium Chloride Oral Solution
Potassium Chloride is indicated for the treatment and prophylaxis of hypokalemia with or without metabolic alkalosis.
February 2, 2021
by expresspharma
Granules India gets USFDA approval of Metformin Hydrochloride ER Tablets
Metformin Hydrochloride ER Tablets are indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus.
January 14, 2021
by expresspharma
Granules gets USFDA nod for ADHD drug dexmethylphenidate HCl extended-release capsules
The drug will be manufactured at the Granules manufacturing facility in Chantilly, Virginia.
September 23, 2020
by expresspharma
Granules Issues Recall of Metformin Hydrochloride Extended-Release Tablets
Granules Pharmaceuticals is voluntarily recalling twelve (12) lots of Metformin Hydrochloride Extended-Release Tablets USP, 750 mg, 100 and 500 count bottles within expiry to the consumer level due to the detection of NNitrosodimethylamine (NDMA) ...
July 21, 2020
by americanpharmaceuticalreview