| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 25000-134-03 | 25000-134 | HUMAN PRESCRIPTION DRUG | Metformin Hydrochloride | Metformin Hydrochloride | TABLET, FILM COATED | ORAL | 20120601 | N/A | ANDA | ANDA090888 | MARKSANS PHARMA LIMITED | METFORMIN HYDROCHLORIDE | 500 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (25000-134-03) |
| 25000-134-14 | 25000-134 | HUMAN PRESCRIPTION DRUG | Metformin Hydrochloride | Metformin Hydrochloride | TABLET, FILM COATED | ORAL | 20120601 | N/A | ANDA | ANDA090888 | MARKSANS PHARMA LIMITED | METFORMIN HYDROCHLORIDE | 500 mg/1 | 1000 TABLET, FILM COATED in 1 BOTTLE (25000-134-14) |
| 25000-134-51 | 25000-134 | HUMAN PRESCRIPTION DRUG | Metformin Hydrochloride | Metformin Hydrochloride | TABLET, FILM COATED | ORAL | 20120601 | N/A | ANDA | ANDA090888 | MARKSANS PHARMA LIMITED | METFORMIN HYDROCHLORIDE | 500 mg/1 | 2600 TABLET, FILM COATED in 1 BAG (25000-134-51) |
| 25000-134-98 | 25000-134 | HUMAN PRESCRIPTION DRUG | Metformin Hydrochloride | Metformin Hydrochloride | TABLET, FILM COATED | ORAL | 20120601 | N/A | ANDA | ANDA090888 | MARKSANS PHARMA LIMITED | METFORMIN HYDROCHLORIDE | 500 mg/1 | 1 BAG in 1 BOX (25000-134-98) / 16455 TABLET, FILM COATED in 1 BAG |