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=ANDA215689"
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
72865-214-30 72865-214 HUMAN PRESCRIPTION DRUG FAMOTIDINE Famotidine TABLET, FILM COATED ORAL 20211015 N/A ANDA ANDA215689 XLCare Pharmaceuticals, Inc. FAMOTIDINE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (72865-214-30)
72865-215-01 72865-215 HUMAN PRESCRIPTION DRUG FAMOTIDINE Famotidine TABLET, FILM COATED ORAL 20211015 N/A ANDA ANDA215689 XLCare Pharmaceuticals, Inc. FAMOTIDINE 40 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (72865-215-01)
72865-215-05 72865-215 HUMAN PRESCRIPTION DRUG FAMOTIDINE Famotidine TABLET, FILM COATED ORAL 20211015 N/A ANDA ANDA215689 XLCare Pharmaceuticals, Inc. FAMOTIDINE 40 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (72865-215-05)
72865-215-18 72865-215 HUMAN PRESCRIPTION DRUG FAMOTIDINE Famotidine TABLET, FILM COATED ORAL 20211015 N/A ANDA ANDA215689 XLCare Pharmaceuticals, Inc. FAMOTIDINE 40 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (72865-215-18)
72865-215-30 72865-215 HUMAN PRESCRIPTION DRUG FAMOTIDINE Famotidine TABLET, FILM COATED ORAL 20211015 N/A ANDA ANDA215689 XLCare Pharmaceuticals, Inc. FAMOTIDINE 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (72865-215-30)
72865-214-18 72865-214 HUMAN PRESCRIPTION DRUG FAMOTIDINE Famotidine TABLET, FILM COATED ORAL 20211015 N/A ANDA ANDA215689 XLCare Pharmaceuticals, Inc. FAMOTIDINE 20 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (72865-214-18)
72865-214-05 72865-214 HUMAN PRESCRIPTION DRUG FAMOTIDINE Famotidine TABLET, FILM COATED ORAL 20211015 N/A ANDA ANDA215689 XLCare Pharmaceuticals, Inc. FAMOTIDINE 20 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (72865-214-05)
72865-214-01 72865-214 HUMAN PRESCRIPTION DRUG FAMOTIDINE Famotidine TABLET, FILM COATED ORAL 20211015 N/A ANDA ANDA215689 XLCare Pharmaceuticals, Inc. FAMOTIDINE 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (72865-214-01)
43602-501-05 43602-501 HUMAN PRESCRIPTION DRUG FAMOTIDINE Famotidine TABLET, FILM COATED ORAL 20211015 N/A ANDA ANDA215689 Ascent Pharmaceuticals, Inc. FAMOTIDINE 20 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (43602-501-05)
43602-501-30 43602-501 HUMAN PRESCRIPTION DRUG FAMOTIDINE Famotidine TABLET, FILM COATED ORAL 20211015 N/A ANDA ANDA215689 Ascent Pharmaceuticals, Inc. FAMOTIDINE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (43602-501-30)
43602-502-05 43602-502 HUMAN PRESCRIPTION DRUG FAMOTIDINE Famotidine TABLET, FILM COATED ORAL 20211015 N/A ANDA ANDA215689 Ascent Pharmaceuticals, Inc. FAMOTIDINE 40 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (43602-502-05)
43602-502-30 43602-502 HUMAN PRESCRIPTION DRUG FAMOTIDINE Famotidine TABLET, FILM COATED ORAL 20211015 N/A ANDA ANDA215689 Ascent Pharmaceuticals, Inc. FAMOTIDINE 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (43602-502-30)
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