商品名 | 申请号 | 产品号 | 申请类型 | 活性成分 | 剂型/给药途径 | 规格/剂量 | RLD | RS | 申请号原始批准/暂定批准日期 | 产品号批准日期 | 申请人 | 市场状态 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
IBUPROFEN AND DIPHENHYDRAMINE CITRATE | 079113 | 001 | ANDA | DIPHENHYDRAMINE CITRATE; IBUPROFEN | TABLET;ORAL | 38MG;200MG | No | No | 2008/12/22 | 2008/12/22 | PERRIGO R AND D | Over-the-counter |
IBUPROFEN AND DIPHENHYDRAMINE CITRATE | 090619 | 001 | ANDA | DIPHENHYDRAMINE CITRATE; IBUPROFEN | TABLET;ORAL | 38MG;200MG | No | No | 2009/07/08 | 2009/07/08 | DR REDDYS LABS LTD | Over-the-counter |
IBUPROFEN AND DIPHENHYDRAMINE CITRATE | 216204 | 001 | ANDA | DIPHENHYDRAMINE CITRATE; IBUPROFEN | TABLET;ORAL | 38MG;200MG | No | No | 2022/05/31 | 2022/05/31 | AUROBINDO PHARMA | Over-the-counter |
IBUPROFEN AND DIPHENHYDRAMINE CITRATE | 211404 | 001 | ANDA | DIPHENHYDRAMINE CITRATE; IBUPROFEN | TABLET;ORAL | 38MG;200MG | No | No | 2024/04/11 | 2024/04/11 | PLD ACQUISITIONS LLC | Over-the-counter |