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=ANDA090365"
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
71335-1486-1 71335-1486 HUMAN PRESCRIPTION DRUG Felodipine Felodipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20200121 N/A ANDA ANDA090365 Bryant Ranch Prepack FELODIPINE 5 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1486-1)
68462-233-01 68462-233 HUMAN PRESCRIPTION DRUG Felodipine Felodipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20101220 N/A ANDA ANDA090365 Glenmark Pharmaceuticals Inc., USA FELODIPINE 2.5 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-233-01)
68462-233-10 68462-233 HUMAN PRESCRIPTION DRUG Felodipine Felodipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20101220 N/A ANDA ANDA090365 Glenmark Pharmaceuticals Inc., USA FELODIPINE 2.5 mg/1 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-233-10)
68462-233-11 68462-233 HUMAN PRESCRIPTION DRUG Felodipine Felodipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20101220 N/A ANDA ANDA090365 Glenmark Pharmaceuticals Inc., USA FELODIPINE 2.5 mg/1 10 BLISTER PACK in 1 CARTON (68462-233-11) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
68462-233-90 68462-233 HUMAN PRESCRIPTION DRUG Felodipine Felodipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20101220 N/A ANDA ANDA090365 Glenmark Pharmaceuticals Inc., USA FELODIPINE 2.5 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-233-90)
68462-234-01 68462-234 HUMAN PRESCRIPTION DRUG Felodipine Felodipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20101220 N/A ANDA ANDA090365 Glenmark Pharmaceuticals Inc., USA FELODIPINE 5 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-234-01)
68462-234-10 68462-234 HUMAN PRESCRIPTION DRUG Felodipine Felodipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20101220 N/A ANDA ANDA090365 Glenmark Pharmaceuticals Inc., USA FELODIPINE 5 mg/1 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-234-10)
68462-234-11 68462-234 HUMAN PRESCRIPTION DRUG Felodipine Felodipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20101220 N/A ANDA ANDA090365 Glenmark Pharmaceuticals Inc., USA FELODIPINE 5 mg/1 10 BLISTER PACK in 1 CARTON (68462-234-11) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
68462-234-90 68462-234 HUMAN PRESCRIPTION DRUG Felodipine Felodipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20101220 N/A ANDA ANDA090365 Glenmark Pharmaceuticals Inc., USA FELODIPINE 5 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-234-90)
68462-235-01 68462-235 HUMAN PRESCRIPTION DRUG Felodipine Felodipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20101220 N/A ANDA ANDA090365 Glenmark Pharmaceuticals Inc., USA FELODIPINE 10 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-235-01)
68462-235-10 68462-235 HUMAN PRESCRIPTION DRUG Felodipine Felodipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20101220 N/A ANDA ANDA090365 Glenmark Pharmaceuticals Inc., USA FELODIPINE 10 mg/1 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-235-10)
68462-235-11 68462-235 HUMAN PRESCRIPTION DRUG Felodipine Felodipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20101220 N/A ANDA ANDA090365 Glenmark Pharmaceuticals Inc., USA FELODIPINE 10 mg/1 10 BLISTER PACK in 1 CARTON (68462-235-11) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
68462-235-90 68462-235 HUMAN PRESCRIPTION DRUG Felodipine Felodipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20101220 N/A ANDA ANDA090365 Glenmark Pharmaceuticals Inc., USA FELODIPINE 10 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-235-90)
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