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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
60505-4518-3 | 60505-4518 | HUMAN PRESCRIPTION DRUG | PAXIL | paroxetine hydrochloride | TABLET, FILM COATED | ORAL | 20190311 | N/A | NDA | NDA020031 | Apotex Corp | PAROXETINE HYDROCHLORIDE | 20 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (60505-4518-3) |
60505-4519-3 | 60505-4519 | HUMAN PRESCRIPTION DRUG | PAXIL | paroxetine hydrochloride | TABLET, FILM COATED | ORAL | 20190311 | N/A | NDA | NDA020031 | Apotex Corp | PAROXETINE HYDROCHLORIDE | 30 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (60505-4519-3) |
60505-4520-3 | 60505-4520 | HUMAN PRESCRIPTION DRUG | PAXIL | paroxetine hydrochloride | TABLET, FILM COATED | ORAL | 20190311 | N/A | NDA | NDA020031 | Apotex Corp | PAROXETINE HYDROCHLORIDE | 40 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (60505-4520-3) |
60505-4517-3 | 60505-4517 | HUMAN PRESCRIPTION DRUG | PAXIL | paroxetine hydrochloride | TABLET, FILM COATED | ORAL | 20190311 | N/A | NDA | NDA020031 | Apotex Corp | PAROXETINE HYDROCHLORIDE | 10 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (60505-4517-3) |