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=ANDA084114"
符合检索条件的记录共 4 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
70518-4294-0 70518-4294 HUMAN PRESCRIPTION DRUG Chlorpromazine Hydrochloride Chlorpromazine Hydrochloride TABLET, FILM COATED ORAL 20250226 N/A ANDA ANDA084114 REMEDYREPACK INC. CHLORPROMAZINE HYDROCHLORIDE 100 mg/1 100 POUCH in 1 BOX (70518-4294-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-4294-1)
0832-6020-00 0832-6020 HUMAN PRESCRIPTION DRUG Chlorpromazine Hydrochloride Chlorpromazine Hydrochloride TABLET, FILM COATED ORAL 20210806 N/A ANDA ANDA084114 Upsher-Smith Laboratories, LLC CHLORPROMAZINE HYDROCHLORIDE 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (0832-6020-00)
0832-6020-01 0832-6020 HUMAN PRESCRIPTION DRUG Chlorpromazine Hydrochloride Chlorpromazine Hydrochloride TABLET, FILM COATED ORAL 20210806 N/A ANDA ANDA084114 Upsher-Smith Laboratories, LLC CHLORPROMAZINE HYDROCHLORIDE 100 mg/1 1 BLISTER PACK in 1 CARTON (0832-6020-01) / 100 TABLET, FILM COATED in 1 BLISTER PACK (0832-6020-89)
0832-6020-10 0832-6020 HUMAN PRESCRIPTION DRUG Chlorpromazine Hydrochloride Chlorpromazine Hydrochloride TABLET, FILM COATED ORAL 20210806 N/A ANDA ANDA084114 Upsher-Smith Laboratories, LLC CHLORPROMAZINE HYDROCHLORIDE 100 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (0832-6020-10)
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