| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 71335-0358-7 | 71335-0358 | HUMAN PRESCRIPTION DRUG | Metronidazole | Metronidazole | TABLET, FILM COATED | ORAL | 20180529 | N/A | ANDA | ANDA203458 | Bryant Ranch Prepack | METRONIDAZOLE | 500 mg/1 | 28 TABLET, FILM COATED in 1 BOTTLE (71335-0358-7) |
| 71335-0358-8 | 71335-0358 | HUMAN PRESCRIPTION DRUG | Metronidazole | Metronidazole | TABLET, FILM COATED | ORAL | 20180612 | N/A | ANDA | ANDA203458 | Bryant Ranch Prepack | METRONIDAZOLE | 500 mg/1 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-0358-8) |
| 71335-0358-9 | 71335-0358 | HUMAN PRESCRIPTION DRUG | Metronidazole | Metronidazole | TABLET, FILM COATED | ORAL | 20190729 | N/A | ANDA | ANDA203458 | Bryant Ranch Prepack | METRONIDAZOLE | 500 mg/1 | 42 TABLET, FILM COATED in 1 BOTTLE (71335-0358-9) |