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=ANDA216994"
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
41226-716-49 41226-716 HUMAN OTC DRUG Dual Action Acetaminophen, Ibuprofen TABLET ORAL 20230711 N/A ANDA ANDA216994 KROGER COMPANY ACETAMINOPHEN; IBUPROFEN 250 mg/1; 125 mg/1 1 BOTTLE in 1 CARTON (41226-716-49) / 144 TABLET in 1 BOTTLE
11673-924-75 11673-924 HUMAN OTC DRUG Dual Action Pain Relief Acetaminophen, Ibuprofen TABLET ORAL 20230711 N/A ANDA ANDA216994 TARGET CORPORATION ACETAMINOPHEN; IBUPROFEN 250 mg/1; 125 mg/1 1 BOTTLE in 1 CARTON (11673-924-75) / 72 TABLET in 1 BOTTLE
25000-080-07 25000-080 HUMAN OTC DRUG Acetaminophen 250 mg and Ibuprofen 125 mg Acetaminophen 250 mg and Ibuprofen 125 mg Tablets TABLET, FILM COATED ORAL 20230711 N/A ANDA ANDA216994 MARKSANS PHARMA LIMITED ACETAMINOPHEN; IBUPROFEN 250 mg/1; 125 mg/1 1 BOTTLE in 1 CARTON (25000-080-07) / 90 TABLET, FILM COATED in 1 BOTTLE
25000-080-72 25000-080 HUMAN OTC DRUG Acetaminophen 250 mg and Ibuprofen 125 mg Acetaminophen 250 mg and Ibuprofen 125 mg Tablets TABLET, FILM COATED ORAL 20230711 N/A ANDA ANDA216994 MARKSANS PHARMA LIMITED ACETAMINOPHEN; IBUPROFEN 250 mg/1; 125 mg/1 1 BOTTLE in 1 CARTON (25000-080-72) / 18 TABLET, FILM COATED in 1 BOTTLE
25000-080-74 25000-080 HUMAN OTC DRUG Acetaminophen 250 mg and Ibuprofen 125 mg Acetaminophen 250 mg and Ibuprofen 125 mg Tablets TABLET, FILM COATED ORAL 20230711 N/A ANDA ANDA216994 MARKSANS PHARMA LIMITED ACETAMINOPHEN; IBUPROFEN 250 mg/1; 125 mg/1 288 TABLET, FILM COATED in 1 BOTTLE (25000-080-74)
21130-716-08 21130-716 HUMAN OTC DRUG Dual Action Acetaminophen, Ibuprofen TABLET ORAL 20230830 N/A ANDA ANDA216994 BETTER LIVING BRANDS, LLC ACETAMINOPHEN; IBUPROFEN 250 mg/1; 125 mg/1 1 BOTTLE in 1 CARTON (21130-716-08) / 18 TABLET in 1 BOTTLE
21130-716-75 21130-716 HUMAN OTC DRUG Dual Action Acetaminophen, Ibuprofen TABLET ORAL 20230830 N/A ANDA ANDA216994 BETTER LIVING BRANDS, LLC ACETAMINOPHEN; IBUPROFEN 250 mg/1; 125 mg/1 1 BOTTLE in 1 CARTON (21130-716-75) / 72 TABLET in 1 BOTTLE
49483-716-49 49483-716 HUMAN OTC DRUG Dual Action Pain Relief Acetaminophen, Ibuprofen TABLET ORAL 20231013 N/A ANDA ANDA216994 TIME CAP LABORATORIES, INC. ACETAMINOPHEN; IBUPROFEN 250 mg/1; 125 mg/1 1 BOTTLE in 1 CARTON (49483-716-49) / 144 TABLET in 1 BOTTLE
49483-716-75 49483-716 HUMAN OTC DRUG Dual Action Pain Relief Acetaminophen, Ibuprofen TABLET ORAL 20231013 N/A ANDA ANDA216994 TIME CAP LABORATORIES, INC. ACETAMINOPHEN; IBUPROFEN 250 mg/1; 125 mg/1 1 BOTTLE in 1 CARTON (49483-716-75) / 72 TABLET in 1 BOTTLE
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