NDC包装代码 | 产品NDC | 产品类型 | 商品名 | 通用名 | 剂型 | 给药途径 | 上市日期 | 结束日期 | 市场类别 | 申请号 | 标签持有者 | 活性成分 | 规格 | 包装描述 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
0591-2411-01 | 0591-2411 | HUMAN PRESCRIPTION DRUG | Metformin Hydrochloride | Metformin Hydrochloride | TABLET, FILM COATED, EXTENDED RELEASE | ORAL | 20170515 | N/A | ANDA | ANDA203755 | Actavis Pharma, Inc. | METFORMIN HYDROCHLORIDE | 500 mg/1 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0591-2411-01) |
0591-2412-19 | 0591-2412 | HUMAN PRESCRIPTION DRUG | Metformin Hydrochloride | Metformin Hydrochloride | TABLET, FILM COATED, EXTENDED RELEASE | ORAL | 20170515 | N/A | ANDA | ANDA203755 | Actavis Pharma, Inc. | METFORMIN HYDROCHLORIDE | 1000 mg/1 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0591-2412-19) |