| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 49884-117-01 | 49884-117 | HUMAN PRESCRIPTION DRUG | Amiloride Hydrochloride | Amiloride Hydrochloride | TABLET | ORAL | 19860512 | N/A | ANDA | ANDA070346 | Par Pharmaceutical, Inc. | AMILORIDE HYDROCHLORIDE ANHYDROUS | 5 mg/1 | 100 TABLET in 1 BOTTLE (49884-117-01) |
| 49884-117-10 | 49884-117 | HUMAN PRESCRIPTION DRUG | Amiloride Hydrochloride | Amiloride Hydrochloride | TABLET | ORAL | 19860512 | N/A | ANDA | ANDA070346 | Par Pharmaceutical, Inc. | AMILORIDE HYDROCHLORIDE ANHYDROUS | 5 mg/1 | 1000 TABLET in 1 BOTTLE (49884-117-10) |
| 63629-2114-1 | 63629-2114 | HUMAN PRESCRIPTION DRUG | Amiloride Hydrochloride | Amiloride Hydrochloride | TABLET | ORAL | 19860512 | N/A | ANDA | ANDA070346 | Bryant Ranch Prepack | AMILORIDE HYDROCHLORIDE ANHYDROUS | 5 mg/1 | 1000 TABLET in 1 BOTTLE (63629-2114-1) |