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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
77771-115-05 | 77771-115 | HUMAN PRESCRIPTION DRUG | Fluoxetine | Fluoxetine Hydrochloride | CAPSULE | ORAL | 20221024 | N/A | ANDA | ANDA204597 | RADHA PHARMACEUTICALS, INC. | FLUOXETINE HYDROCHLORIDE | 40 mg/1 | 500 CAPSULE in 1 BOTTLE (77771-115-05) |
71205-974-60 | 71205-974 | HUMAN PRESCRIPTION DRUG | Fluoxetine | Fluoxetine Hydrochloride | CAPSULE | ORAL | 20200507 | N/A | ANDA | ANDA204597 | Proficient Rx LP | FLUOXETINE HYDROCHLORIDE | 10 mg/1 | 60 CAPSULE in 1 BOTTLE (71205-974-60) |
71205-974-72 | 71205-974 | HUMAN PRESCRIPTION DRUG | Fluoxetine | Fluoxetine Hydrochloride | CAPSULE | ORAL | 20200507 | N/A | ANDA | ANDA204597 | Proficient Rx LP | FLUOXETINE HYDROCHLORIDE | 10 mg/1 | 120 CAPSULE in 1 BOTTLE (71205-974-72) |
71205-974-90 | 71205-974 | HUMAN PRESCRIPTION DRUG | Fluoxetine | Fluoxetine Hydrochloride | CAPSULE | ORAL | 20200507 | N/A | ANDA | ANDA204597 | Proficient Rx LP | FLUOXETINE HYDROCHLORIDE | 10 mg/1 | 90 CAPSULE in 1 BOTTLE (71205-974-90) |