| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 71205-522-42 | 71205-522 | HUMAN PRESCRIPTION DRUG | Ibuprofen | Ibuprofen | TABLET, FILM COATED | ORAL | 20240801 | N/A | ANDA | ANDA078329 | Proficient Rx LP | IBUPROFEN | 600 mg/1 | 42 TABLET, FILM COATED in 1 BOTTLE (71205-522-42) |
| 71205-522-60 | 71205-522 | HUMAN PRESCRIPTION DRUG | Ibuprofen | Ibuprofen | TABLET, FILM COATED | ORAL | 20250519 | N/A | ANDA | ANDA078329 | Proficient Rx LP | IBUPROFEN | 600 mg/1 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-522-60) |
| 71205-522-90 | 71205-522 | HUMAN PRESCRIPTION DRUG | Ibuprofen | Ibuprofen | TABLET, FILM COATED | ORAL | 20250519 | N/A | ANDA | ANDA078329 | Proficient Rx LP | IBUPROFEN | 600 mg/1 | 90 TABLET, FILM COATED in 1 BOTTLE (71205-522-90) |