| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 71335-1530-4 | 71335-1530 | HUMAN PRESCRIPTION DRUG | Finasteride | Finasteride | TABLET, FILM COATED | ORAL | 20200320 | N/A | ANDA | ANDA078341 | Bryant Ranch Prepack | FINASTERIDE | 5 mg/1 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-1530-4) |
| 71335-1530-5 | 71335-1530 | HUMAN PRESCRIPTION DRUG | Finasteride | Finasteride | TABLET, FILM COATED | ORAL | 20211228 | N/A | ANDA | ANDA078341 | Bryant Ranch Prepack | FINASTERIDE | 5 mg/1 | 500 TABLET, FILM COATED in 1 BOTTLE (71335-1530-5) |
| 71335-1530-6 | 71335-1530 | HUMAN PRESCRIPTION DRUG | Finasteride | Finasteride | TABLET, FILM COATED | ORAL | 20211228 | N/A | ANDA | ANDA078341 | Bryant Ranch Prepack | FINASTERIDE | 5 mg/1 | 180 TABLET, FILM COATED in 1 BOTTLE (71335-1530-6) |