| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 72189-372-30 | 72189-372 | HUMAN PRESCRIPTION DRUG | Carvedilol | Carvedilol | TABLET, FILM COATED | ORAL | 20220810 | N/A | ANDA | ANDA078227 | Direct_Rx | CARVEDILOL | 12.5 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (72189-372-30) |
| 0781-5224-01 | 0781-5224 | HUMAN PRESCRIPTION DRUG | Carvedilol | Carvedilol | TABLET, FILM COATED | ORAL | 20070905 | 20260831 | ANDA | ANDA078227 | Sandoz Inc | CARVEDILOL | 25 mg/1 | 100 TABLET, FILM COATED in 1 BOTTLE (0781-5224-01) |
| 0781-5223-01 | 0781-5223 | HUMAN PRESCRIPTION DRUG | Carvedilol | Carvedilol | TABLET, FILM COATED | ORAL | 20070905 | 20260831 | ANDA | ANDA078227 | Sandoz Inc | CARVEDILOL | 12.5 mg/1 | 100 TABLET, FILM COATED in 1 BOTTLE (0781-5223-01) |
| 0781-5221-01 | 0781-5221 | HUMAN PRESCRIPTION DRUG | Carvedilol | Carvedilol | TABLET, FILM COATED | ORAL | 20070905 | 20260630 | ANDA | ANDA078227 | Sandoz Inc | CARVEDILOL | 3.125 mg/1 | 100 TABLET, FILM COATED in 1 BOTTLE (0781-5221-01) |