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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
71610-055-60 | 71610-055 | HUMAN PRESCRIPTION DRUG | Nifedipine | Nifedipine | TABLET, EXTENDED RELEASE | ORAL | 20180502 | N/A | ANDA | ANDA076070 | Aphena Pharma Solutions - Tennessee, LLC | NIFEDIPINE | 90 mg/1 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-055-60) |
72162-2261-1 | 72162-2261 | HUMAN PRESCRIPTION DRUG | Nifedipine | Nifedipine | TABLET, EXTENDED RELEASE | ORAL | 20240223 | N/A | ANDA | ANDA076070 | Bryant Ranch Prepack | NIFEDIPINE | 90 mg/1 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-2261-1) |
68682-107-10 | 68682-107 | HUMAN PRESCRIPTION DRUG | Nifedipine | Nifedipine | TABLET, EXTENDED RELEASE | ORAL | 20020816 | N/A | ANDA | ANDA076070 | Oceanside Pharmaceuticals | NIFEDIPINE | 90 mg/1 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68682-107-10) |