| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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) |
| 71205-804-30 | 71205-804 | HUMAN PRESCRIPTION DRUG | Imipramine Hydrochloride | Imipramine Hydrochloride | TABLET, FILM COATED | ORAL | 20230605 | N/A | ANDA | ANDA040903 | Proficient Rx LP | IMIPRAMINE HYDROCHLORIDE | 10 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-804-30) |
| 71205-804-60 | 71205-804 | HUMAN PRESCRIPTION DRUG | Imipramine Hydrochloride | Imipramine Hydrochloride | TABLET, FILM COATED | ORAL | 20230605 | N/A | ANDA | ANDA040903 | Proficient Rx LP | IMIPRAMINE HYDROCHLORIDE | 10 mg/1 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-804-60) |
| 71205-804-90 | 71205-804 | HUMAN PRESCRIPTION DRUG | Imipramine Hydrochloride | Imipramine Hydrochloride | TABLET, FILM COATED | ORAL | 20230605 | N/A | ANDA | ANDA040903 | Proficient Rx LP | IMIPRAMINE HYDROCHLORIDE | 10 mg/1 | 90 TABLET, FILM COATED in 1 BOTTLE (71205-804-90) |