| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 69452-191-17 | 69452-191 | HUMAN PRESCRIPTION DRUG | ivabradine | ivabradine | TABLET, FILM COATED | ORAL | 20250301 | N/A | ANDA | ANDA213276 | Bionpharma Inc. | IVABRADINE HYDROCHLORIDE | 7.5 mg/1 | 60 TABLET, FILM COATED in 1 BOTTLE (69452-191-17) |
| 69452-191-30 | 69452-191 | HUMAN PRESCRIPTION DRUG | ivabradine | ivabradine | TABLET, FILM COATED | ORAL | 20250301 | N/A | ANDA | ANDA213276 | Bionpharma Inc. | IVABRADINE HYDROCHLORIDE | 7.5 mg/1 | 500 TABLET, FILM COATED in 1 BOTTLE (69452-191-30) |
| 69452-190-17 | 69452-190 | HUMAN PRESCRIPTION DRUG | ivabradine | ivabradine | TABLET, FILM COATED | ORAL | 20250301 | N/A | ANDA | ANDA213276 | Bionpharma Inc. | IVABRADINE HYDROCHLORIDE | 5 mg/1 | 60 TABLET, FILM COATED in 1 BOTTLE (69452-190-17) |
| 69452-190-30 | 69452-190 | HUMAN PRESCRIPTION DRUG | ivabradine | ivabradine | TABLET, FILM COATED | ORAL | 20250301 | N/A | ANDA | ANDA213276 | Bionpharma Inc. | IVABRADINE HYDROCHLORIDE | 5 mg/1 | 500 TABLET, FILM COATED in 1 BOTTLE (69452-190-30) |