WebJul 7, 2024 · Recall of metformin hydrochloride extended-Release tablets USP 750 mg by Granules Pharmaceuticals due to N-Nitrosodimethylamine (NDMA). More on the FDA website. Alert covering recent metformin extended-release recalls.
Metformin Recalled for Possible Cancerous Chemical
WebGranules Pharmaceuticals, Inc., Chantilly, VA is voluntarily recalling twelve (12) lots of Metformin Hydrochloride Extended-Release Tablets USP, 750 mg, 100 and 500 count bottles within expiry to ... WebThe last Recall Enforcement Report for Metformin with NDC 70010-491 was initiated on 07-03-2024 as a Class II recall and it is currently ongoing. Search. ... 100 ct. bottle (NDC 70010-492-01) and 500 ct. bottle (NDC 70010-492-05), Manufactured for: Granules Pharmaceutical Inc., Chantilly, VA, Manufactured by: Granules India Limited, Hyderabad ... iqas application status
Recall Subscriber Alert Emails - California State Board of Pharmacy
WebJun 25, 2024 · If you filled Metformin extended-release tablets 500mg, 750mg or 1,000mg at a RETAIL or MTF pharmacy, please contact that pharmacy directly for next steps. See letter sent to beneficiaries impacted with a filled medication about the details of the recall. WebSep 26, 2024 · The Food and Drug Administration issued a notice given by Viona Pharmaceuticals, Inc. on January 7, 2024. Viona Pharmaceuticals is voluntarily recalling 23 lots of Metformin Hydrochloride Extended-Release Tablets, USP 750 mg. The impacted batches of metformin were found to have high levels of N-nitrosodimethylamine, or NDMA. WebMetformin has some minor side effects. The most common side effects (which occur in roughly 5% of people taking the drug) include: Diarrhea. Hypoglycemia (low blood sugar) Nausea. Other less common side effects include: Asthenia (weakness or lack of energy) Indigestion. Abdominal discomfort. orchid growers canada