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=ANDA075400"
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
70677-1102-2 70677-1102 HUMAN OTC DRUG foster and thrive acid reducer Famotidine TABLET, FILM COATED ORAL 20230719 N/A ANDA ANDA075400 Strategic Sourcing Services LLC FAMOTIDINE 10 mg/1 1 BOTTLE in 1 CARTON (70677-1102-2) / 60 TABLET, FILM COATED in 1 BOTTLE
70677-1102-3 70677-1102 HUMAN OTC DRUG foster and thrive acid reducer Famotidine TABLET, FILM COATED ORAL 20230719 N/A ANDA ANDA075400 Strategic Sourcing Services LLC FAMOTIDINE 10 mg/1 1 BOTTLE in 1 CARTON (70677-1102-3) / 90 TABLET, FILM COATED in 1 BOTTLE
59779-141-39 59779-141 HUMAN OTC DRUG acid controller original strength Famotidine TABLET, FILM COATED ORAL 20150924 N/A ANDA ANDA075400 CVS Pharmacy FAMOTIDINE 10 mg/1 1 BOTTLE in 1 CARTON (59779-141-39) / 30 TABLET, FILM COATED in 1 BOTTLE
59779-141-75 59779-141 HUMAN OTC DRUG acid controller original strength Famotidine TABLET, FILM COATED ORAL 20091017 N/A ANDA ANDA075400 CVS Pharmacy FAMOTIDINE 10 mg/1 1 BOTTLE in 1 CARTON (59779-141-75) / 90 TABLET, FILM COATED in 1 BOTTLE
55910-141-60 55910-141 HUMAN OTC DRUG dg health heartburn prevention original strength Famotidine TABLET, FILM COATED ORAL 20100310 N/A ANDA ANDA075400 Dolgencorp, LLC FAMOTIDINE 10 mg/1 20 BLISTER PACK in 1 CARTON (55910-141-60) / 1 TABLET, FILM COATED in 1 BLISTER PACK
55910-141-72 55910-141 HUMAN OTC DRUG dg health heartburn prevention original strength Famotidine TABLET, FILM COATED ORAL 20200122 N/A ANDA ANDA075400 Dolgencorp, LLC FAMOTIDINE 10 mg/1 1 BOTTLE in 1 CARTON (55910-141-72) / 60 TABLET, FILM COATED in 1 BOTTLE
55910-141-75 55910-141 HUMAN OTC DRUG dg health heartburn prevention original strength Famotidine TABLET, FILM COATED ORAL 20200122 N/A ANDA ANDA075400 Dolgencorp, LLC FAMOTIDINE 10 mg/1 1 BOTTLE in 1 CARTON (55910-141-75) / 90 TABLET, FILM COATED in 1 BOTTLE
63187-999-10 63187-999 HUMAN OTC DRUG heartburn relief original strength Famotidine TABLET ORAL 20180402 N/A ANDA ANDA075400 Proficient Rx LP FAMOTIDINE 10 mg/1 10 TABLET in 1 BOTTLE (63187-999-10)
63187-999-30 63187-999 HUMAN OTC DRUG heartburn relief original strength Famotidine TABLET ORAL 20180402 N/A ANDA ANDA075400 Proficient Rx LP FAMOTIDINE 10 mg/1 30 TABLET in 1 BOTTLE (63187-999-30)
63187-999-60 63187-999 HUMAN OTC DRUG heartburn relief original strength Famotidine TABLET ORAL 20180402 N/A ANDA ANDA075400 Proficient Rx LP FAMOTIDINE 10 mg/1 60 TABLET in 1 BOTTLE (63187-999-60)
63187-999-90 63187-999 HUMAN OTC DRUG heartburn relief original strength Famotidine TABLET ORAL 20180402 N/A ANDA ANDA075400 Proficient Rx LP FAMOTIDINE 10 mg/1 90 TABLET in 1 BOTTLE (63187-999-90)
56062-141-65 56062-141 HUMAN OTC DRUG acid reducer Famotidine TABLET, FILM COATED ORAL 20091123 N/A ANDA ANDA075400 Publix Super Markets Inc FAMOTIDINE 10 mg/1 30 BLISTER PACK in 1 CARTON (56062-141-65) / 1 TABLET, FILM COATED in 1 BLISTER PACK
0363-0141-39 0363-0141 HUMAN OTC DRUG Acid Controller Original Strength Famotidine TABLET, FILM COATED ORAL 20260116 N/A ANDA ANDA075400 Walgreen Company FAMOTIDINE 10 mg/1 1 BOTTLE in 1 CARTON (0363-0141-39) / 30 TABLET, FILM COATED in 1 BOTTLE
0363-0141-48 0363-0141 HUMAN OTC DRUG Acid Controller Original Strength Famotidine TABLET, FILM COATED ORAL 20251212 N/A ANDA ANDA075400 Walgreen Company FAMOTIDINE 10 mg/1 2 BOTTLE in 1 CARTON (0363-0141-48) / 90 TABLET, FILM COATED in 1 BOTTLE
0363-0141-75 0363-0141 HUMAN OTC DRUG Acid Controller Original Strength Famotidine TABLET, FILM COATED ORAL 20090828 N/A ANDA ANDA075400 Walgreen Company FAMOTIDINE 10 mg/1 1 BOTTLE in 1 CARTON (0363-0141-75) / 90 TABLET, FILM COATED in 1 BOTTLE
37808-301-65 37808-301 HUMAN OTC DRUG acid controller Famotidine TABLET, FILM COATED ORAL 20151023 N/A ANDA ANDA075400 H E B FAMOTIDINE 10 mg/1 30 BLISTER PACK in 1 CARTON (37808-301-65) / 1 TABLET, FILM COATED in 1 BLISTER PACK
37808-301-72 37808-301 HUMAN OTC DRUG acid controller Famotidine TABLET, FILM COATED ORAL 20151023 N/A ANDA ANDA075400 H E B FAMOTIDINE 10 mg/1 1 BOTTLE in 1 CARTON (37808-301-72) / 60 TABLET, FILM COATED in 1 BOTTLE
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase