| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 50090-3148-0 | 50090-3148 | HUMAN PRESCRIPTION DRUG | Imipramine Hydrochloride | Imipramine Hydrochloride | TABLET, FILM COATED | ORAL | 20171003 | N/A | ANDA | ANDA040903 | A-S Medication Solutions | IMIPRAMINE HYDROCHLORIDE | 25 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-3148-0) |
| 70518-1588-0 | 70518-1588 | HUMAN PRESCRIPTION DRUG | Imipramine Hydrochloride | Imipramine Hydrochloride | TABLET, FILM COATED | ORAL | 20181025 | N/A | ANDA | ANDA040903 | REMEDYREPACK INC. | IMIPRAMINE HYDROCHLORIDE | 50 mg/1 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1588-0) |
| 69315-134-01 | 69315-134 | HUMAN PRESCRIPTION DRUG | Imipramine Hydrochloride | Imipramine Hydrochloride | TABLET, FILM COATED | ORAL | 20160412 | N/A | ANDA | ANDA040903 | Leading Pharma, LLC | IMIPRAMINE HYDROCHLORIDE | 25 mg/1 | 100 TABLET, FILM COATED in 1 BOTTLE (69315-134-01) |
| 69315-134-10 | 69315-134 | HUMAN PRESCRIPTION DRUG | Imipramine Hydrochloride | Imipramine Hydrochloride | TABLET, FILM COATED | ORAL | 20160501 | N/A | ANDA | ANDA040903 | Leading Pharma, LLC | IMIPRAMINE HYDROCHLORIDE | 25 mg/1 | 1000 TABLET, FILM COATED in 1 BOTTLE (69315-134-10) |