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Tag: recall

You Searched For "recall"
Rs 1 Cr Plus Earners in Firing Line as Dr Reddys Targets 25% Cost Cut, May Shut Digital Unit

Dr Reddy's Labs recalls over 3 lakh bottles of Cinacalcet tablets in US over manufacturing issues

Ruchika Sharma5 Nov 2024 1:30 PM IST
New Delhi: Dr Reddy's Laboratories is recalling over 3.3 lakh bottles of Cinacalcet tablets, a medication used for treatment of high calcium...
Lupin recalls over 2000 bottles of antidepressant medication in US

Lupin, Dr Reddy's Labs recall products in US over manufacturing issues: USFDA

Ruchika Sharma5 Sept 2024 1:30 PM IST
New Delhi: Pharma majors Lupin, Dr Reddy's Laboratories are recalling products in the US over manufacturing issues, according to a latest...
Sun Pharma, Zydus and Glenmark recall various products in US over manufacturing issues

Baxter Healthcare issues Voluntary Recall for Tisseel LYO Fibrin Sealant Kits Over Quality Concerns

Dr. Divya Colin3 Sept 2024 6:00 PM IST
New Delhi: The Drug Controller General of India has issued a notice regarding the urgent voluntary recall made by Baxter Healthcare for the 4 mL and...
Sun Pharma, Zydus and Glenmark recall various products in US over manufacturing issues

Aurobindo Pharma, Glenmark and 1 other recall products in US market over production issue: USFDA

Ruchika Sharma27 Aug 2024 12:30 PM IST
New Delhi: Aurobindo Pharma, Glenmark, and FDC Ltd. are recalling certain products in the United States over manufacturing issues, according to the US...
Sun Pharma, Zydus and Glenmark recall various products in US over manufacturing issues

Glenmark Pharma recalls 114 batches of hypokalemia drug Potassium Chloride Extended Release in US

Ruchika Sharma27 Jun 2024 12:20 PM IST
Mahwah: Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ is voluntarily recalling 114 batches of Potassium Chloride Extended-Release Capsules, USP (750...
FDC recalls over 60000 bottles of Timolol Maleate Ophthalmic Solution  in US

Sun Pharma, Dr Reddy's Labs, Aurobindo recall products in US over manufacturing issues

Ruchika Sharma20 May 2024 12:50 PM IST
New Delhi: According to the latest Enforcement Report from the US Food and Drug Administration (USFDA), pharmaceutical companies Dr Reddy's...
Lupin recalls over 2000 bottles of antidepressant medication in US

Cipla, Glenmark recall products from American market over manufacturing issues

Ruchika Sharma6 May 2024 11:09 AM IST
New Delhi: Glenmark and Cipla are recalling products from the American market over manufacturing issues, as per the US health regulator.According to...
Dr Reddys Gets SEC Nod for Higher Semaglutide Dose in Ongoing Phase III Study, Govt Sites Mandated

Dr Reddy's recalls six lots of Sapropterin Dihydrochloride Powder for Oral Solution 100 mg over sub potency

Ruchika Sharma24 April 2024 1:10 PM IST
Hyderabad, Princeton: Dr Reddy's Laboratories Ltd. has announced that it is voluntarily recalling six (6) lots of Sapropterin...
Lupin recalls over 2000 bottles of antidepressant medication in US

Glenmark Pharma recalls 6528 bottles of BP drug in US

Ruchika Sharma15 April 2024 1:36 PM IST
New Delhi: Glenmark Pharmaceuticals is recalling 6,528 bottles of a medication prescribed for the treatment of high blood pressure in the...
Sun Pharma concludes acquisition of Checkpoint Therapeutics

Sun Pharma recalls 55000 bottles of generic drug to treat gout from American market

Ruchika Sharma12 March 2024 1:13 PM IST
The affected lot was produced at Sun Pharma's Dadra-based plant for Memphis-based Northstar Rx LLC, the US regulator noted.
Lupin recalls over 2000 bottles of antidepressant medication in US

Sun Pharma unit recalls over 54000 bottles of Mesalamine ER capsules in US

Ruchika Sharma9 March 2024 11:24 AM IST
The affected lot of capsules have been manufactured by Sun Pharmaceutical Industries at its Mohali-based manufacturing plant and distributed in the US...
FDC recalls over 60000 bottles of Timolol Maleate Ophthalmic Solution  in US

Philips recall of imaging machines classified as most serious by USFDA

Ruchika Sharma16 Feb 2024 1:30 PM IST
There has been one incident related to use of the device, but no reports of injuries or deaths, the FDA said.
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