| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 45963-709-11 | 45963-709 | HUMAN PRESCRIPTION DRUG | metoprolol succinate | metoprolol succinate | TABLET, FILM COATED, EXTENDED RELEASE | ORAL | 20191023 | N/A | ANDA | ANDA204161 | Actavis Pharma, Inc. | METOPROLOL SUCCINATE | 25 mg/1 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (45963-709-11) |
| 45963-709-96 | 45963-709 | HUMAN PRESCRIPTION DRUG | metoprolol succinate | metoprolol succinate | TABLET, FILM COATED, EXTENDED RELEASE | ORAL | 20191023 | N/A | ANDA | ANDA204161 | Actavis Pharma, Inc. | METOPROLOL SUCCINATE | 25 mg/1 | 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (45963-709-96) |