| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 0093-0017-01 | 0093-0017 | HUMAN PRESCRIPTION DRUG | Moexipril Hydrochloride | Moexipril Hydrochloride | TABLET, FILM COATED | ORAL | 20030508 | N/A | ANDA | ANDA076204 | Teva Pharmaceuticals USA, Inc. | MOEXIPRIL HYDROCHLORIDE | 7.5 mg/1 | 100 TABLET, FILM COATED in 1 BOTTLE (0093-0017-01) |
| 0093-5150-01 | 0093-5150 | HUMAN PRESCRIPTION DRUG | Moexipril Hydrochloride | Moexipril Hydrochloride | TABLET, FILM COATED | ORAL | 20030508 | N/A | ANDA | ANDA076204 | Teva Pharmaceuticals USA, Inc. | MOEXIPRIL HYDROCHLORIDE | 15 mg/1 | 100 TABLET, FILM COATED in 1 BOTTLE (0093-5150-01) |