| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 49884-468-11 | 49884-468 | HUMAN PRESCRIPTION DRUG | Fluoxetine | Fluoxetine | TABLET, FILM COATED | ORAL | 20171116 | N/A | ANDA | ANDA209419 | Par Pharmaceutical, Inc. | FLUOXETINE HYDROCHLORIDE | 60 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (49884-468-11) |
| 63629-2201-1 | 63629-2201 | HUMAN PRESCRIPTION DRUG | Fluoxetine | Fluoxetine | TABLET, FILM COATED | ORAL | 20221028 | N/A | ANDA | ANDA209419 | Bryant Ranch Prepack | FLUOXETINE HYDROCHLORIDE | 60 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-2201-1) |
| 72162-1506-3 | 72162-1506 | HUMAN PRESCRIPTION DRUG | Fluoxetine | Fluoxetine | TABLET, FILM COATED | ORAL | 20240408 | N/A | ANDA | ANDA209419 | Bryant Ranch Prepack | FLUOXETINE HYDROCHLORIDE | 60 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (72162-1506-3) |