| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 0591-0404-01 | 0591-0404 | HUMAN PRESCRIPTION DRUG | Verapamil Hydrochloride | Verapamil Hydrochloride | TABLET, FILM COATED | ORAL | 19930629 | N/A | ANDA | ANDA072924 | Actavis Pharma, Inc. | VERAPAMIL HYDROCHLORIDE | 40 mg/1 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-0404-01) |
| 71335-2087-1 | 71335-2087 | HUMAN PRESCRIPTION DRUG | Verapamil Hydrochloride | Verapamil Hydrochloride | TABLET, FILM COATED | ORAL | 20220516 | N/A | ANDA | ANDA072924 | Bryant Ranch Prepack | VERAPAMIL HYDROCHLORIDE | 40 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2087-1) |