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=ANDA216592"
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
11822-1131-4 11822-1131 HUMAN OTC DRUG Acetaminophen and Ibuprofen (NSAID) Acetaminophen and Ibuprofen (NSAID) TABLET ORAL 20230721 N/A ANDA ANDA216592 RITE AID ACETAMINOPHEN; IBUPROFEN 250 mg/1; 125 mg/1 144 TABLET in 1 BOTTLE (11822-1131-4)
11822-1131-6 11822-1131 HUMAN OTC DRUG Acetaminophen and Ibuprofen (NSAID) Acetaminophen and Ibuprofen (NSAID) TABLET ORAL 20230721 N/A ANDA ANDA216592 RITE AID ACETAMINOPHEN; IBUPROFEN 250 mg/1; 125 mg/1 216 TABLET in 1 BOTTLE (11822-1131-6)
70010-131-26 70010-131 HUMAN OTC DRUG Acetaminophen and Ibuprofen Acetaminophen and Ibuprofen TABLET ORAL 20230724 N/A ANDA ANDA216592 Granules Pharmaceuticals Inc. ACETAMINOPHEN; IBUPROFEN 250 mg/1; 125 mg/1 1 BOTTLE in 1 CARTON (70010-131-26) / 18 TABLET in 1 BOTTLE
70010-131-31 70010-131 HUMAN OTC DRUG Acetaminophen and Ibuprofen Acetaminophen and Ibuprofen TABLET ORAL 20230724 N/A ANDA ANDA216592 Granules Pharmaceuticals Inc. ACETAMINOPHEN; IBUPROFEN 250 mg/1; 125 mg/1 288 TABLET in 1 BOTTLE (70010-131-31)
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