美国药品NDC(国家药品编码)与药品说明书数据库(U.S. FDA National Drug Code DataBase)
检索条件:" 注册申请号=ANDA076006"
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
70518-3937-0 70518-3937 HUMAN PRESCRIPTION DRUG Fluoxetine Fluoxetine TABLET, FILM COATED ORAL 20231206 N/A ANDA ANDA076006 REMEDYREPACK INC. FLUOXETINE HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3937-0)
43598-566-01 43598-566 HUMAN PRESCRIPTION DRUG Fluoxetine Fluoxetine TABLET, FILM COATED ORAL 20180508 N/A ANDA ANDA076006 Dr.Reddy's Laboratories Inc. FLUOXETINE HYDROCHLORIDE 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (43598-566-01)
43598-566-10 43598-566 HUMAN PRESCRIPTION DRUG Fluoxetine Fluoxetine TABLET, FILM COATED ORAL 20180508 N/A ANDA ANDA076006 Dr.Reddy's Laboratories Inc. FLUOXETINE HYDROCHLORIDE 20 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (43598-566-10)
43598-566-30 43598-566 HUMAN PRESCRIPTION DRUG Fluoxetine Fluoxetine TABLET, FILM COATED ORAL 20180508 N/A ANDA ANDA076006 Dr.Reddy's Laboratories Inc. FLUOXETINE HYDROCHLORIDE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (43598-566-30)
16714-113-02 16714-113 HUMAN PRESCRIPTION DRUG Fluoxetine Fluoxetine TABLET, FILM COATED ORAL 20190918 N/A ANDA ANDA076006 NorthStar Rx LLC FLUOXETINE HYDROCHLORIDE 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (16714-113-02)
16714-113-01 16714-113 HUMAN PRESCRIPTION DRUG Fluoxetine Fluoxetine TABLET, FILM COATED ORAL 20190918 N/A ANDA ANDA076006 NorthStar Rx LLC FLUOXETINE HYDROCHLORIDE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (16714-113-01)
55111-150-01 55111-150 HUMAN PRESCRIPTION DRUG Fluoxetine Fluoxetine TABLET, FILM COATED ORAL 20160930 N/A ANDA ANDA076006 Dr.Reddy's Laboratories Limited FLUOXETINE HYDROCHLORIDE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (55111-150-01)
55111-150-05 55111-150 HUMAN PRESCRIPTION DRUG Fluoxetine Fluoxetine TABLET, FILM COATED ORAL 20160930 N/A ANDA ANDA076006 Dr.Reddy's Laboratories Limited FLUOXETINE HYDROCHLORIDE 10 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (55111-150-05)
55111-150-10 55111-150 HUMAN PRESCRIPTION DRUG Fluoxetine Fluoxetine TABLET, FILM COATED ORAL 20160930 N/A ANDA ANDA076006 Dr.Reddy's Laboratories Limited FLUOXETINE HYDROCHLORIDE 10 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (55111-150-10)
55111-150-30 55111-150 HUMAN PRESCRIPTION DRUG Fluoxetine Fluoxetine TABLET, FILM COATED ORAL 20160930 N/A ANDA ANDA076006 Dr.Reddy's Laboratories Limited FLUOXETINE HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (55111-150-30)
55111-150-78 55111-150 HUMAN PRESCRIPTION DRUG Fluoxetine Fluoxetine TABLET, FILM COATED ORAL 20160930 N/A ANDA ANDA076006 Dr.Reddy's Laboratories Limited FLUOXETINE HYDROCHLORIDE 10 mg/1 10 BLISTER PACK in 1 CARTON (55111-150-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (55111-150-79)
16714-112-01 16714-112 HUMAN PRESCRIPTION DRUG Fluoxetine Fluoxetine TABLET, FILM COATED ORAL 20190918 N/A ANDA ANDA076006 NorthStar Rx LLC FLUOXETINE HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (16714-112-01)
16714-112-02 16714-112 HUMAN PRESCRIPTION DRUG Fluoxetine Fluoxetine TABLET, FILM COATED ORAL 20190918 N/A ANDA ANDA076006 NorthStar Rx LLC FLUOXETINE HYDROCHLORIDE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (16714-112-02)
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