| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 63629-2079-1 | 63629-2079 | HUMAN PRESCRIPTION DRUG | AMPHETAMINE SULFATE | amphetamine sulfate | TABLET | ORAL | 20240402 | N/A | ANDA | ANDA212901 | Bryant Ranch Prepack | AMPHETAMINE SULFATE | 5 mg/1 | 100 TABLET in 1 BOTTLE (63629-2079-1) |
| 0527-2524-37 | 0527-2524 | HUMAN PRESCRIPTION DRUG | AMPHETAMINE SULFATE | amphetamine sulfate | TABLET | ORAL | 20200601 | N/A | ANDA | ANDA212901 | Lannett Company, Inc. | AMPHETAMINE SULFATE | 5 mg/1 | 100 TABLET in 1 BOTTLE (0527-2524-37) |
| 72162-1087-1 | 72162-1087 | HUMAN PRESCRIPTION DRUG | AMPHETAMINE SULFATE | amphetamine sulfate | TABLET | ORAL | 20240405 | N/A | ANDA | ANDA212901 | Bryant Ranch Prepack | AMPHETAMINE SULFATE | 5 mg/1 | 100 TABLET in 1 BOTTLE (72162-1087-1) |
| 0527-2525-37 | 0527-2525 | HUMAN PRESCRIPTION DRUG | AMPHETAMINE SULFATE | amphetamine sulfate | TABLET | ORAL | 20200601 | N/A | ANDA | ANDA212901 | Lannett Company, Inc. | AMPHETAMINE SULFATE | 10 mg/1 | 100 TABLET in 1 BOTTLE (0527-2525-37) |
| 63629-2078-1 | 63629-2078 | HUMAN PRESCRIPTION DRUG | AMPHETAMINE SULFATE | amphetamine sulfate | TABLET | ORAL | 20211221 | N/A | ANDA | ANDA212901 | Bryant Ranch Prepack | AMPHETAMINE SULFATE | 10 mg/1 | 100 TABLET in 1 BOTTLE (63629-2078-1) |
| 72162-1088-1 | 72162-1088 | HUMAN PRESCRIPTION DRUG | AMPHETAMINE SULFATE | amphetamine sulfate | TABLET | ORAL | 20240405 | N/A | ANDA | ANDA212901 | Bryant Ranch Prepack | AMPHETAMINE SULFATE | 10 mg/1 | 100 TABLET in 1 BOTTLE (72162-1088-1) |