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=ANDA090796"
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
60760-603-90 60760-603 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20230206 N/A ANDA ANDA090796 St. Mary's Medical Park Pharmacy IBUPROFEN 600 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-603-90)
71335-1517-1 71335-1517 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20200220 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 400 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71335-1517-1)
71335-1517-2 71335-1517 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20200220 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 400 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-1517-2)
71335-1517-3 71335-1517 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20200220 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 400 mg/1 40 TABLET, FILM COATED in 1 BOTTLE (71335-1517-3)
71335-1517-4 71335-1517 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20200220 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 400 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-1517-4)
71335-1517-5 71335-1517 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20200220 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 400 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-1517-5)
71335-1517-6 71335-1517 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20200220 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 400 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71335-1517-6)
71335-1517-7 71335-1517 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20200220 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 400 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (71335-1517-7)
71335-1517-8 71335-1517 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20200220 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 400 mg/1 21 TABLET, FILM COATED in 1 BOTTLE (71335-1517-8)
71335-1517-9 71335-1517 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20200220 N/A ANDA ANDA090796 Bryant Ranch Prepack IBUPROFEN 400 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (71335-1517-9)
68788-7745-8 68788-7745 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20200701 N/A ANDA ANDA090796 Preferred Pharmaceuticals, Inc. IBUPROFEN 400 mg/1 28 TABLET, FILM COATED in 1 BOTTLE (68788-7745-8)
68788-7745-9 68788-7745 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20200701 N/A ANDA ANDA090796 Preferred Pharmaceuticals, Inc. IBUPROFEN 400 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68788-7745-9)
72189-266-15 72189-266 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20210916 N/A ANDA ANDA090796 DIRECT RX IBUPROFEN 800 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (72189-266-15)
72189-266-30 72189-266 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20210916 N/A ANDA ANDA090796 DIRECT RX IBUPROFEN 800 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (72189-266-30)
72189-266-40 72189-266 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20210916 N/A ANDA ANDA090796 DIRECT RX IBUPROFEN 800 mg/1 40 TABLET, FILM COATED in 1 BOTTLE (72189-266-40)
72189-266-60 72189-266 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20210916 N/A ANDA ANDA090796 DIRECT RX IBUPROFEN 800 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (72189-266-60)
72189-266-71 72189-266 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20210916 N/A ANDA ANDA090796 DIRECT RX IBUPROFEN 800 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (72189-266-71)
72189-266-72 72189-266 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20210916 N/A ANDA ANDA090796 DIRECT RX IBUPROFEN 800 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (72189-266-72)
72189-266-90 72189-266 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20210916 N/A ANDA ANDA090796 DIRECT RX IBUPROFEN 800 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (72189-266-90)
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