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=ANDA084113"
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
0832-6019-00 0832-6019 HUMAN PRESCRIPTION DRUG Chlorpromazine Hydrochloride Chlorpromazine Hydrochloride TABLET, FILM COATED ORAL 20210806 N/A ANDA ANDA084113 Upsher-Smith Laboratories, LLC CHLORPROMAZINE HYDROCHLORIDE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (0832-6019-00)
0832-6019-01 0832-6019 HUMAN PRESCRIPTION DRUG Chlorpromazine Hydrochloride Chlorpromazine Hydrochloride TABLET, FILM COATED ORAL 20210806 N/A ANDA ANDA084113 Upsher-Smith Laboratories, LLC CHLORPROMAZINE HYDROCHLORIDE 50 mg/1 1 BLISTER PACK in 1 CARTON (0832-6019-01) / 100 TABLET, FILM COATED in 1 BLISTER PACK (0832-6019-89)
0832-6019-10 0832-6019 HUMAN PRESCRIPTION DRUG Chlorpromazine Hydrochloride Chlorpromazine Hydrochloride TABLET, FILM COATED ORAL 20210806 N/A ANDA ANDA084113 Upsher-Smith Laboratories, LLC CHLORPROMAZINE HYDROCHLORIDE 50 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (0832-6019-10)
70518-3674-2 70518-3674 HUMAN PRESCRIPTION DRUG Chlorpromazine Hydrochloride Chlorpromazine Hydrochloride TABLET, FILM COATED ORAL 20231204 N/A ANDA ANDA084113 REMEDYREPACK INC. CHLORPROMAZINE HYDROCHLORIDE 50 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3674-2)
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