| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 71335-9692-4 | 71335-9692 | HUMAN PRESCRIPTION DRUG | PRAVASTATIN SODIUM | PRAVASTATIN SODIUM | TABLET | ORAL | 20230418 | N/A | ANDA | ANDA209869 | Bryant Ranch Prepack | PRAVASTATIN SODIUM | 20 mg/1 | 60 TABLET in 1 BOTTLE (71335-9692-4) |
| 70377-048-12 | 70377-048 | HUMAN PRESCRIPTION DRUG | Pravastatin sodium | Pravastatin sodium | TABLET | ORAL | 20210201 | N/A | ANDA | ANDA209869 | Biocon Pharma Inc. | PRAVASTATIN SODIUM | 80 mg/1 | 90 TABLET in 1 BOTTLE (70377-048-12) |
| 70377-048-13 | 70377-048 | HUMAN PRESCRIPTION DRUG | Pravastatin sodium | Pravastatin sodium | TABLET | ORAL | 20210201 | N/A | ANDA | ANDA209869 | Biocon Pharma Inc. | PRAVASTATIN SODIUM | 80 mg/1 | 500 TABLET in 1 BOTTLE (70377-048-13) |
| 70377-047-14 | 70377-047 | HUMAN PRESCRIPTION DRUG | Pravastatin sodium | Pravastatin sodium | TABLET | ORAL | 20210201 | N/A | ANDA | ANDA209869 | Biocon Pharma Inc. | PRAVASTATIN SODIUM | 40 mg/1 | 1000 TABLET in 1 BOTTLE (70377-047-14) |
| 70377-048-11 | 70377-048 | HUMAN PRESCRIPTION DRUG | Pravastatin sodium | Pravastatin sodium | TABLET | ORAL | 20210201 | N/A | ANDA | ANDA209869 | Biocon Pharma Inc. | PRAVASTATIN SODIUM | 80 mg/1 | 30 TABLET in 1 BOTTLE (70377-048-11) |