Teva Pharmaceuticals USA, Inc. Initiates Voluntary Nationwide Recall of Metformin Hydrochloride Extended-Release Tablets USP 500 mg and 750 mg Due to Detection of N-Nitrosodimethylamine (NDMA) - CÔNG TY CỔ PHẦN DƯỢC PHẨM
Teva 00093726701 - McKesson Medical-Surgical
Teva Pharmaceuticals USA, Inc. Initiates Voluntary Nationwide Recall of Metformin Hydrochloride Extended-Release Tablets USP 500 mg and 750 mg Due to Detection of N-Nitrosodimethylamine (NDMA) | FDA
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Recall of three batches of Metformin-Teva 500mg Tablets (with photo)
Teva recalls 14 lots of tablets due to NDMA detection | WWMT