| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 72789-493-01 | 72789-493 | HUMAN PRESCRIPTION DRUG | Imipramine Hydrochloride | Imipramine Hydrochloride | TABLET, FILM COATED | ORAL | 20250903 | N/A | ANDA | ANDA040903 | PD-Rx Pharmaceuticals, Inc. | IMIPRAMINE HYDROCHLORIDE | 50 mg/1 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-493-01) |
| 72789-493-95 | 72789-493 | HUMAN PRESCRIPTION DRUG | Imipramine Hydrochloride | Imipramine Hydrochloride | TABLET, FILM COATED | ORAL | 20250310 | N/A | ANDA | ANDA040903 | PD-Rx Pharmaceuticals, Inc. | IMIPRAMINE HYDROCHLORIDE | 50 mg/1 | 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-493-95) |