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=ANDA213368"
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
70710-1133-1 70710-1133 HUMAN PRESCRIPTION DRUG Chlorpromazine hydrochloride Chlorpromazine hydrochloride TABLET, FILM COATED ORAL 20200127 N/A ANDA ANDA213368 Zydus Pharmaceuticals (USA) Inc. CHLORPROMAZINE HYDROCHLORIDE 200 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70710-1133-1)
70710-1133-4 70710-1133 HUMAN PRESCRIPTION DRUG Chlorpromazine hydrochloride Chlorpromazine hydrochloride TABLET, FILM COATED ORAL 20200127 N/A ANDA ANDA213368 Zydus Pharmaceuticals (USA) Inc. CHLORPROMAZINE HYDROCHLORIDE 200 mg/1 10 BLISTER PACK in 1 CARTON (70710-1133-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70710-1133-2)
16714-047-01 16714-047 HUMAN PRESCRIPTION DRUG Chlorpromazine hydrochloride Chlorpromazine hydrochloride TABLET, FILM COATED ORAL 20200511 N/A ANDA ANDA213368 Northstar Rx LLC CHLORPROMAZINE HYDROCHLORIDE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (16714-047-01)
70710-1131-1 70710-1131 HUMAN PRESCRIPTION DRUG Chlorpromazine hydrochloride Chlorpromazine hydrochloride TABLET, FILM COATED ORAL 20200127 N/A ANDA ANDA213368 Zydus Pharmaceuticals (USA) Inc. CHLORPROMAZINE HYDROCHLORIDE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70710-1131-1)
70710-1131-4 70710-1131 HUMAN PRESCRIPTION DRUG Chlorpromazine hydrochloride Chlorpromazine hydrochloride TABLET, FILM COATED ORAL 20200127 N/A ANDA ANDA213368 Zydus Pharmaceuticals (USA) Inc. CHLORPROMAZINE HYDROCHLORIDE 50 mg/1 10 BLISTER PACK in 1 CARTON (70710-1131-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70710-1131-2)
70771-1509-1 70771-1509 HUMAN PRESCRIPTION DRUG Chlorpromazine hydrochloride Chlorpromazine hydrochloride TABLET, FILM COATED ORAL 20200127 N/A ANDA ANDA213368 Zydus Lifesciences Limited CHLORPROMAZINE HYDROCHLORIDE 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70771-1509-1)
70771-1509-4 70771-1509 HUMAN PRESCRIPTION DRUG Chlorpromazine hydrochloride Chlorpromazine hydrochloride TABLET, FILM COATED ORAL 20200127 N/A ANDA ANDA213368 Zydus Lifesciences Limited CHLORPROMAZINE HYDROCHLORIDE 100 mg/1 10 BLISTER PACK in 1 CARTON (70771-1509-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1509-2)
0904-7131-61 0904-7131 HUMAN PRESCRIPTION DRUG Chlorpromazine hydrochloride Chlorpromazine hydrochloride TABLET, FILM COATED ORAL 20200127 N/A ANDA ANDA213368 Major Pharmaceuticals CHLORPROMAZINE HYDROCHLORIDE 50 mg/1 100 BLISTER PACK in 1 CARTON (0904-7131-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK
16714-048-01 16714-048 HUMAN PRESCRIPTION DRUG Chlorpromazine hydrochloride Chlorpromazine hydrochloride TABLET, FILM COATED ORAL 20200511 N/A ANDA ANDA213368 Northstar Rx LLC CHLORPROMAZINE HYDROCHLORIDE 25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (16714-048-01)
70710-1132-1 70710-1132 HUMAN PRESCRIPTION DRUG Chlorpromazine hydrochloride Chlorpromazine hydrochloride TABLET, FILM COATED ORAL 20200127 N/A ANDA ANDA213368 Zydus Pharmaceuticals (USA) Inc. CHLORPROMAZINE HYDROCHLORIDE 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70710-1132-1)
70710-1132-4 70710-1132 HUMAN PRESCRIPTION DRUG Chlorpromazine hydrochloride Chlorpromazine hydrochloride TABLET, FILM COATED ORAL 20200127 N/A ANDA ANDA213368 Zydus Pharmaceuticals (USA) Inc. CHLORPROMAZINE HYDROCHLORIDE 100 mg/1 10 BLISTER PACK in 1 CARTON (70710-1132-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70710-1132-2)
70710-1130-1 70710-1130 HUMAN PRESCRIPTION DRUG Chlorpromazine hydrochloride Chlorpromazine hydrochloride TABLET, FILM COATED ORAL 20200127 N/A ANDA ANDA213368 Zydus Pharmaceuticals (USA) Inc. CHLORPROMAZINE HYDROCHLORIDE 25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70710-1130-1)
70710-1130-4 70710-1130 HUMAN PRESCRIPTION DRUG Chlorpromazine hydrochloride Chlorpromazine hydrochloride TABLET, FILM COATED ORAL 20200127 N/A ANDA ANDA213368 Zydus Pharmaceuticals (USA) Inc. CHLORPROMAZINE HYDROCHLORIDE 25 mg/1 10 BLISTER PACK in 1 CARTON (70710-1130-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70710-1130-2)
70771-1508-1 70771-1508 HUMAN PRESCRIPTION DRUG Chlorpromazine hydrochloride Chlorpromazine hydrochloride TABLET, FILM COATED ORAL 20200127 N/A ANDA ANDA213368 Zydus Lifesciences Limited CHLORPROMAZINE HYDROCHLORIDE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70771-1508-1)
70771-1508-4 70771-1508 HUMAN PRESCRIPTION DRUG Chlorpromazine hydrochloride Chlorpromazine hydrochloride TABLET, FILM COATED ORAL 20200127 N/A ANDA ANDA213368 Zydus Lifesciences Limited CHLORPROMAZINE HYDROCHLORIDE 50 mg/1 10 BLISTER PACK in 1 CARTON (70771-1508-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1508-2)
0904-7130-06 0904-7130 HUMAN PRESCRIPTION DRUG Chlorpromazine hydrochloride Chlorpromazine hydrochloride TABLET, FILM COATED ORAL 20200127 N/A ANDA ANDA213368 Major Pharmaceuticals CHLORPROMAZINE HYDROCHLORIDE 25 mg/1 50 BLISTER PACK in 1 CARTON (0904-7130-06) / 1 TABLET, FILM COATED in 1 BLISTER PACK
0904-7130-61 0904-7130 HUMAN PRESCRIPTION DRUG Chlorpromazine hydrochloride Chlorpromazine hydrochloride TABLET, FILM COATED ORAL 20200127 N/A ANDA ANDA213368 Major Pharmaceuticals CHLORPROMAZINE HYDROCHLORIDE 25 mg/1 100 BLISTER PACK in 1 CARTON (0904-7130-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK
70518-3348-0 70518-3348 HUMAN PRESCRIPTION DRUG Chlorpromazine hydrochloride Chlorpromazine hydrochloride TABLET, FILM COATED ORAL 20220128 N/A ANDA ANDA213368 REMEDYREPACK INC. CHLORPROMAZINE HYDROCHLORIDE 50 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3348-0)
16714-051-01 16714-051 HUMAN PRESCRIPTION DRUG Chlorpromazine hydrochloride Chlorpromazine hydrochloride TABLET, FILM COATED ORAL 20200511 N/A ANDA ANDA213368 Northstar Rx LLC CHLORPROMAZINE HYDROCHLORIDE 200 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (16714-051-01)
70771-1506-1 70771-1506 HUMAN PRESCRIPTION DRUG Chlorpromazine hydrochloride Chlorpromazine hydrochloride TABLET, FILM COATED ORAL 20200127 N/A ANDA ANDA213368 Zydus Lifesciences Limited CHLORPROMAZINE HYDROCHLORIDE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70771-1506-1)
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