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=NDA020325"
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
16837-889-20 16837-889 HUMAN OTC DRUG Maximum Strength PEPCID AC Icy Cool Mint Famotidine TABLET, FILM COATED ORAL 20240311 N/A NDA NDA020325 Kenvue Brands LLC FAMOTIDINE 20 mg/1 1 BOTTLE in 1 CARTON (16837-889-20) / 20 TABLET, FILM COATED in 1 BOTTLE
16837-889-40 16837-889 HUMAN OTC DRUG Maximum Strength PEPCID AC Icy Cool Mint Famotidine TABLET, FILM COATED ORAL 20240311 N/A NDA NDA020325 Kenvue Brands LLC FAMOTIDINE 20 mg/1 1 BOTTLE in 1 CARTON (16837-889-40) / 40 TABLET, FILM COATED in 1 BOTTLE
66715-9748-8 66715-9748 HUMAN OTC DRUG Pepcid AC Famotidine TABLET, FILM COATED ORAL 20200401 N/A NDA NDA020325 Lil' Drug Store Products, Inc. FAMOTIDINE 20 mg/1 5 BLISTER PACK in 1 CARTON (66715-9748-8) / 1 TABLET, FILM COATED in 1 BLISTER PACK
16837-855-50 16837-855 HUMAN OTC DRUG PEPCID AC Maximum Strength Famotidine TABLET, FILM COATED ORAL 20030901 N/A NDA NDA020325 Kenvue Brands LLC FAMOTIDINE 20 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (16837-855-50) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
16837-855-52 16837-855 HUMAN OTC DRUG PEPCID AC Maximum Strength Famotidine TABLET, FILM COATED ORAL 20030901 N/A NDA NDA020325 Kenvue Brands LLC FAMOTIDINE 20 mg/1 50 POUCH in 1 TRAY (16837-855-52) / 1 TABLET, FILM COATED in 1 POUCH
16837-855-70 16837-855 HUMAN OTC DRUG PEPCID AC Maximum Strength Famotidine TABLET, FILM COATED ORAL 20030901 N/A NDA NDA020325 Kenvue Brands LLC FAMOTIDINE 20 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (16837-855-70) / 70 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
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