| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 16714-114-01 | 16714-114 | HUMAN PRESCRIPTION DRUG | Fluoxetine hydrochloride | Fluoxetine hydrochloride | TABLET, FILM COATED | ORAL; ORAL | 20190918 | N/A | ANDA | ANDA211721 | NorthStar Rx LLC | FLUOXETINE HYDROCHLORIDE | 60 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (16714-114-01) |
| 43598-632-01 | 43598-632 | HUMAN PRESCRIPTION DRUG | Fluoxetine hydrochloride | Fluoxetine hydrochloride | TABLET, FILM COATED | ORAL | 20190128 | N/A | ANDA | ANDA211721 | Dr. Reddy's Laboratories Inc. | FLUOXETINE HYDROCHLORIDE | 60 mg/1 | 100 TABLET, FILM COATED in 1 BOTTLE (43598-632-01) |
| 43598-632-30 | 43598-632 | HUMAN PRESCRIPTION DRUG | Fluoxetine hydrochloride | Fluoxetine hydrochloride | TABLET, FILM COATED | ORAL | 20190128 | N/A | ANDA | ANDA211721 | Dr. Reddy's Laboratories Inc. | FLUOXETINE HYDROCHLORIDE | 60 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (43598-632-30) |