| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 63187-022-90 | 63187-022 | HUMAN PRESCRIPTION DRUG | Ibuprofen | Ibuprofen | TABLET | ORAL | 20140501 | N/A | ANDA | ANDA078558 | Proficient Rx LP | IBUPROFEN | 800 mg/1 | 90 TABLET in 1 BOTTLE (63187-022-90) |
| 63187-022-20 | 63187-022 | HUMAN PRESCRIPTION DRUG | Ibuprofen | Ibuprofen | TABLET | ORAL | 20160901 | N/A | ANDA | ANDA078558 | Proficient Rx LP | IBUPROFEN | 800 mg/1 | 20 TABLET in 1 BOTTLE (63187-022-20) |
| 63187-022-21 | 63187-022 | HUMAN PRESCRIPTION DRUG | Ibuprofen | Ibuprofen | TABLET | ORAL | 20170901 | N/A | ANDA | ANDA078558 | Proficient Rx LP | IBUPROFEN | 800 mg/1 | 21 TABLET in 1 BOTTLE (63187-022-21) |
| 63187-022-30 | 63187-022 | HUMAN PRESCRIPTION DRUG | Ibuprofen | Ibuprofen | TABLET | ORAL | 20140501 | N/A | ANDA | ANDA078558 | Proficient Rx LP | IBUPROFEN | 800 mg/1 | 30 TABLET in 1 BOTTLE (63187-022-30) |
| 50090-6616-0 | 50090-6616 | HUMAN PRESCRIPTION DRUG | Ibuprofen | Ibuprofen | TABLET | ORAL | 20230824 | N/A | ANDA | ANDA078558 | A-S Medication Solutions | IBUPROFEN | 800 mg/1 | 90 TABLET in 1 BOTTLE (50090-6616-0) |