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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
63187-731-30 | 63187-731 | HUMAN PRESCRIPTION DRUG | Pravastatin sodium | Pravastatin sodium | TABLET | ORAL | 20160701 | N/A | ANDA | ANDA076939 | Proficient Rx LP | PRAVASTATIN SODIUM | 20 mg/1 | 30 TABLET in 1 BOTTLE (63187-731-30) |
63187-731-60 | 63187-731 | HUMAN PRESCRIPTION DRUG | Pravastatin sodium | Pravastatin sodium | TABLET | ORAL | 20160701 | N/A | ANDA | ANDA076939 | Proficient Rx LP | PRAVASTATIN SODIUM | 20 mg/1 | 60 TABLET in 1 BOTTLE (63187-731-60) |
63187-731-90 | 63187-731 | HUMAN PRESCRIPTION DRUG | Pravastatin sodium | Pravastatin sodium | TABLET | ORAL | 20160701 | N/A | ANDA | ANDA076939 | Proficient Rx LP | PRAVASTATIN SODIUM | 20 mg/1 | 90 TABLET in 1 BOTTLE (63187-731-90) |
63187-732-30 | 63187-732 | HUMAN PRESCRIPTION DRUG | Pravastatin sodium | Pravastatin sodium | TABLET | ORAL | 20160701 | N/A | ANDA | ANDA076939 | Proficient Rx LP | PRAVASTATIN SODIUM | 40 mg/1 | 30 TABLET in 1 BOTTLE (63187-732-30) |
63187-732-60 | 63187-732 | HUMAN PRESCRIPTION DRUG | Pravastatin sodium | Pravastatin sodium | TABLET | ORAL | 20160701 | N/A | ANDA | ANDA076939 | Proficient Rx LP | PRAVASTATIN SODIUM | 40 mg/1 | 60 TABLET in 1 BOTTLE (63187-732-60) |
63187-732-90 | 63187-732 | HUMAN PRESCRIPTION DRUG | Pravastatin sodium | Pravastatin sodium | TABLET | ORAL | 20160701 | N/A | ANDA | ANDA076939 | Proficient Rx LP | PRAVASTATIN SODIUM | 40 mg/1 | 90 TABLET in 1 BOTTLE (63187-732-90) |