美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=DIPHENHYDRAMINE HYDROCHLORIDE"
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
BROMODIPHENHYDRAMINE HYDROCHLORIDE AND CODEINE PHOSPHATE 088626 001 ANDA BROMODIPHENHYDRAMINE HYDROCHLORIDE; CODEINE PHOSPHATE SYRUP;ORAL 12.5MG/5ML;10MG/5ML No No 1984/10/12 1984/10/12 WOCKHARDT Discontinued
DIPHENHYDRAMINE HYDROCHLORIDE 089488 001 ANDA DIPHENHYDRAMINE HYDROCHLORIDE CAPSULE;ORAL 25MG No No 1987/01/02 1987/01/02 SUN PHARM INDUSTRIES Discontinued
DIPHENHYDRAMINE HYDROCHLORIDE 089489 001 ANDA DIPHENHYDRAMINE HYDROCHLORIDE CAPSULE;ORAL 50MG No No 1987/01/02 1987/01/02 SUN PHARM INDUSTRIES Discontinued
DIPHENHYDRAMINE HYDROCHLORIDE 072416 001 ANDA DIPHENHYDRAMINE HYDROCHLORIDE SYRUP;ORAL 12.5MG/5ML No No 1990/09/28 1990/09/28 SCIEGEN PHARMS INC Discontinued
DIPHENHYDRAMINE HYDROCHLORIDE 040140 001 ANDA DIPHENHYDRAMINE HYDROCHLORIDE INJECTABLE;INJECTION 50MG/ML No No 1998/11/20 1998/11/20 HOSPIRA Discontinued
DIPHENHYDRAMINE HYDROCHLORIDE 040466 001 ANDA DIPHENHYDRAMINE HYDROCHLORIDE INJECTABLE;INJECTION 50MG/ML No No 2002/05/28 2002/05/28 APP PHARMS Prescription
DIPHENHYDRAMINE HYDROCHLORIDE 040498 001 ANDA DIPHENHYDRAMINE HYDROCHLORIDE INJECTABLE;INJECTION 50MG/ML No Yes 2005/07/12 2005/07/12 MYLAN INSTITUTIONAL Prescription
IBUPROFEN AND DIPHENHYDRAMINE HYDROCHLORIDE 090397 001 ANDA DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN CAPSULE;ORAL 25MG;EQ 200MG FREE ACID AND POTASSIUM SALT No No 2010/11/22 2010/11/22 BIONPHARMA Over-the-counter
IBUPROFEN AND DIPHENHYDRAMINE HYDROCHLORIDE 200888 001 ANDA DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN CAPSULE;ORAL 25MG;EQ 200MG FREE ACID AND POTASSIUM SALT No No 2012/03/05 2012/03/05 STRIDES SOFTGELS Over-the-counter
DIPHENHYDRAMINE HYDROCHLORIDE PRESERVATIVE FREE 091526 001 ANDA DIPHENHYDRAMINE HYDROCHLORIDE INJECTABLE;INJECTION 50MG/ML No No 2013/03/26 2013/03/26 FRESENIUS KABI USA Prescription
DIPHENHYDRAMINE HYDROCHLORIDE 205723 001 ANDA DIPHENHYDRAMINE HYDROCHLORIDE INJECTABLE;INJECTION 50MG/ML No No 2018/08/22 2018/08/22 MICRO LABS Prescription
NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE 209726 001 ANDA DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM TABLET;ORAL 25MG;220MG No No 2018/10/23 2018/10/23 AMNEAL PHARMS CO Over-the-counter
NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE 207597 001 ANDA DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM TABLET;ORAL 25MG;220MG No No 2019/01/25 2019/01/25 P AND L Discontinued
IBUPROFEN AND DIPHENHYDRAMINE HYDROCHLORIDE 210676 001 ANDA DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN CAPSULE;ORAL 25MG;EQ 200MG FREE ACID AND POTASSIUM SALT No No 2019/02/14 2019/02/14 AUROBINDO PHARMA LTD Over-the-counter
NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE 208499 001 ANDA DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM TABLET;ORAL 25MG;220MG No No 2019/05/10 2019/05/10 PERRIGO R AND D Over-the-counter
NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE 211830 001 ANDA DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM TABLET;ORAL 25MG;220MG No No 2019/08/22 2019/08/22 COREPHARMA Over-the-counter
NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE 213663 001 ANDA DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM TABLET;ORAL 25MG;220MG No No 2020/09/24 2020/09/24 GRANULES Over-the-counter
DIPHENHYDRAMINE HYDROCHLORIDE 218448 001 ANDA DIPHENHYDRAMINE HYDROCHLORIDE INJECTABLE;INJECTION 50MG/ML No No 2024/03/20 2024/03/20 GLAND PHARMA LTD Prescription
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