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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
70518-3931-0 | 70518-3931 | HUMAN PRESCRIPTION DRUG | TADALAFIL | tadalafil | TABLET | ORAL | 20231204 | N/A | ANDA | ANDA210608 | REMEDYREPACK INC. | TADALAFIL | 20 mg/1 | 12 TABLET in 1 BOTTLE, PLASTIC (70518-3931-0) |
70518-3931-1 | 70518-3931 | HUMAN PRESCRIPTION DRUG | TADALAFIL | tadalafil | TABLET | ORAL | 20231207 | N/A | ANDA | ANDA210608 | REMEDYREPACK INC. | TADALAFIL | 20 mg/1 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-3931-1) |
43547-990-06 | 43547-990 | HUMAN PRESCRIPTION DRUG | TADALAFIL | tadalafil | TABLET | ORAL | 20220811 | N/A | ANDA | ANDA210608 | Solco Healthcare US, LLC | TADALAFIL | 20 mg/1 | 60 TABLET in 1 BOTTLE (43547-990-06) |
43547-990-50 | 43547-990 | HUMAN PRESCRIPTION DRUG | TADALAFIL | tadalafil | TABLET | ORAL | 20220811 | N/A | ANDA | ANDA210608 | Solco Healthcare US, LLC | TADALAFIL | 20 mg/1 | 500 TABLET in 1 BOTTLE (43547-990-50) |