| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 72189-535-30 | 72189-535 | HUMAN PRESCRIPTION DRUG | Amantadine HCL | Amantadine HCL | TABLET | ORAL | 20240223 | N/A | ANDA | ANDA209035 | Direct_Rx | AMANTADINE HYDROCHLORIDE | 100 mg/1 | 30 TABLET in 1 BOTTLE (72189-535-30) |
| 72189-535-90 | 72189-535 | HUMAN PRESCRIPTION DRUG | Amantadine HCL | Amantadine HCL | TABLET | ORAL | 20240223 | N/A | ANDA | ANDA209035 | Direct_Rx | AMANTADINE HYDROCHLORIDE | 100 mg/1 | 90 TABLET in 1 BOTTLE (72189-535-90) |
| 42543-497-01 | 42543-497 | HUMAN PRESCRIPTION DRUG | Amantadine Hydrochloride | Amantadine Hydrochloride | TABLET | ORAL | 20170804 | N/A | ANDA | ANDA209035 | Strides Pharma Inc. | AMANTADINE HYDROCHLORIDE | 100 mg/1 | 100 TABLET in 1 BOTTLE (42543-497-01) |
| 42543-497-05 | 42543-497 | HUMAN PRESCRIPTION DRUG | Amantadine Hydrochloride | Amantadine Hydrochloride | TABLET | ORAL | 20170808 | N/A | ANDA | ANDA209035 | Strides Pharma Inc. | AMANTADINE HYDROCHLORIDE | 100 mg/1 | 500 TABLET in 1 BOTTLE (42543-497-05) |