| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 71205-674-03 | 71205-674 | HUMAN PRESCRIPTION DRUG | Azithromycin | Azithromycin | TABLET, FILM COATED | ORAL | 20220707 | N/A | ANDA | ANDA065212 | Proficient Rx LP | AZITHROMYCIN DIHYDRATE | 500 mg/1 | 1 DOSE PACK in 1 CARTON (71205-674-03) / 3 TABLET, FILM COATED in 1 DOSE PACK |
| 67296-1430-2 | 67296-1430 | HUMAN PRESCRIPTION DRUG | Azithromycin | Azithromycin | TABLET, FILM COATED | ORAL | 20190214 | N/A | ANDA | ANDA065212 | RedPharm Drug | AZITHROMYCIN DIHYDRATE | 500 mg/1 | 2 TABLET, FILM COATED in 1 BLISTER PACK (67296-1430-2) |
| 0781-8090-31 | 0781-8090 | HUMAN PRESCRIPTION DRUG | Azithromycin | Azithromycin | TABLET, FILM COATED | ORAL | 20190214 | N/A | ANDA | ANDA065212 | Sandoz Inc | AZITHROMYCIN DIHYDRATE | 500 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (0781-8090-31) |
| 0781-8090-03 | 0781-8090 | HUMAN PRESCRIPTION DRUG | Azithromycin | Azithromycin | TABLET, FILM COATED | ORAL | 20190214 | N/A | ANDA | ANDA065212 | Sandoz Inc | AZITHROMYCIN DIHYDRATE | 500 mg/1 | 1 DOSE PACK in 1 CARTON (0781-8090-03) / 3 TABLET, FILM COATED in 1 DOSE PACK |