| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 0480-7270-98 | 0480-7270 | HUMAN PRESCRIPTION DRUG | Pravastatin Sodium | Pravastatin Sodium | TABLET | ORAL | 20230209 | N/A | ANDA | ANDA077793 | Teva Pharmaceuticals, Inc. | PRAVASTATIN SODIUM | 80 mg/1 | 90 TABLET in 1 BOTTLE (0480-7270-98) |
| 0480-7270-10 | 0480-7270 | HUMAN PRESCRIPTION DRUG | Pravastatin Sodium | Pravastatin Sodium | TABLET | ORAL | 20230320 | N/A | ANDA | ANDA077793 | Teva Pharmaceuticals, Inc. | PRAVASTATIN SODIUM | 80 mg/1 | 1000 TABLET in 1 BOTTLE (0480-7270-10) |
| 84386-034-99 | 84386-034 | HUMAN PRESCRIPTION DRUG | Pravastatin sodium | Pravastatin sodium | TABLET | ORAL | 20250227 | N/A | ANDA | ANDA077793 | Aurobindo Pharma Limited | PRAVASTATIN SODIUM | 80 mg/1 | 1000 TABLET in 1 BOTTLE (84386-034-99) |
| 84386-034-90 | 84386-034 | HUMAN PRESCRIPTION DRUG | Pravastatin sodium | Pravastatin sodium | TABLET | ORAL | 20250227 | N/A | ANDA | ANDA077793 | Aurobindo Pharma Limited | PRAVASTATIN SODIUM | 80 mg/1 | 90 TABLET in 1 BOTTLE (84386-034-90) |