| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 70518-4543-0 | 70518-4543 | HUMAN PRESCRIPTION DRUG | Fluoxetine | Fluoxetine | CAPSULE | ORAL | 20260107 | N/A | ANDA | ANDA078619 | REMEDYREPACK INC. | FLUOXETINE HYDROCHLORIDE | 20 mg/1 | 30 CAPSULE in 1 BLISTER PACK (70518-4543-0) |
| 70518-4543-1 | 70518-4543 | HUMAN PRESCRIPTION DRUG | Fluoxetine | Fluoxetine | CAPSULE | ORAL | 20260423 | N/A | ANDA | ANDA078619 | REMEDYREPACK INC. | FLUOXETINE HYDROCHLORIDE | 20 mg/1 | 50 POUCH in 1 BOX (70518-4543-1) / 1 CAPSULE in 1 POUCH (70518-4543-2) |
| 72603-489-01 | 72603-489 | HUMAN PRESCRIPTION DRUG | Fluoxetine | Fluoxetine | CAPSULE | ORAL | 20250901 | N/A | ANDA | ANDA078619 | NorthStar Rx LLC | FLUOXETINE HYDROCHLORIDE | 20 mg/1 | 100 CAPSULE in 1 BOTTLE (72603-489-01) |
| 72603-489-02 | 72603-489 | HUMAN PRESCRIPTION DRUG | Fluoxetine | Fluoxetine | CAPSULE | ORAL | 20250901 | N/A | ANDA | ANDA078619 | NorthStar Rx LLC | FLUOXETINE HYDROCHLORIDE | 20 mg/1 | 1000 CAPSULE in 1 BOTTLE (72603-489-02) |
| 82009-100-10 | 82009-100 | HUMAN PRESCRIPTION DRUG | Fluoxetine | Fluoxetine Hydrochloride | CAPSULE | ORAL | 20230901 | N/A | ANDA | ANDA078619 | QUALLENT PHARMACEUTICALS HEALTH LLC | FLUOXETINE HYDROCHLORIDE | 10 mg/1 | 1000 CAPSULE in 1 BOTTLE (82009-100-10) |