| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 50090-5766-1 | 50090-5766 | HUMAN PRESCRIPTION DRUG | Amiodarone Hydrochloride | Amiodarone Hydrochloride | TABLET | ORAL | 20211004 | N/A | ANDA | ANDA213446 | A-S Medication Solutions | AMIODARONE HYDROCHLORIDE | 200 mg/1 | 30 TABLET in 1 BOTTLE (50090-5766-1) |
| 50090-5766-2 | 50090-5766 | HUMAN PRESCRIPTION DRUG | Amiodarone Hydrochloride | Amiodarone Hydrochloride | TABLET | ORAL | 20211007 | N/A | ANDA | ANDA213446 | A-S Medication Solutions | AMIODARONE HYDROCHLORIDE | 200 mg/1 | 90 TABLET in 1 BOTTLE (50090-5766-2) |
| 29300-359-05 | 29300-359 | HUMAN PRESCRIPTION DRUG | Amiodarone Hydrochloride | Amiodarone Hydrochloride | TABLET | ORAL | 20200901 | N/A | ANDA | ANDA213446 | Unichem Pharmaceuticals (USA), Inc. | AMIODARONE HYDROCHLORIDE | 200 mg/1 | 500 TABLET in 1 BOTTLE (29300-359-05) |
| 29300-359-16 | 29300-359 | HUMAN PRESCRIPTION DRUG | Amiodarone Hydrochloride | Amiodarone Hydrochloride | TABLET | ORAL | 20200901 | N/A | ANDA | ANDA213446 | Unichem Pharmaceuticals (USA), Inc. | AMIODARONE HYDROCHLORIDE | 200 mg/1 | 60 TABLET in 1 BOTTLE (29300-359-16) |