| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 47781-600-30 | 47781-600 | HUMAN PRESCRIPTION DRUG | Fluoxetine Hydrochloride | Fluoxetine Hydrochloride | TABLET, FILM COATED | ORAL | 20170901 | 20240701 | NDA AUTHORIZED GENERIC | NDA202133 | Alvogen Inc. | FLUOXETINE HYDROCHLORIDE | 60 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (47781-600-30) |
| 24979-255-06 | 24979-255 | HUMAN PRESCRIPTION DRUG | Fluoxetine HCl | Fluoxetine HCl | TABLET, FILM COATED | ORAL | 20240115 | N/A | NDA | NDA202133 | TWi Pharmaceuticals, Inc. | FLUOXETINE HYDROCHLORIDE | 60 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (24979-255-06) |
| 52427-576-30 | 52427-576 | HUMAN PRESCRIPTION DRUG | Fluoxetine HCl | Fluoxetine HCl | TABLET, FILM COATED | ORAL | 20170901 | 20260401 | NDA | NDA202133 | Almatica Pharma Inc. | FLUOXETINE HYDROCHLORIDE | 60 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (52427-576-30) |