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）

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
70710-1129-1	70710-1129	HUMAN PRESCRIPTION DRUG	Chlorpromazine hydrochloride	Chlorpromazine hydrochloride	TABLET, FILM COATED	ORAL	20200127	N/A	ANDA	ANDA213368	Zydus Pharmaceuticals (USA) Inc.	CHLORPROMAZINE HYDROCHLORIDE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70710-1129-1)
70710-1129-4	70710-1129	HUMAN PRESCRIPTION DRUG	Chlorpromazine hydrochloride	Chlorpromazine hydrochloride	TABLET, FILM COATED	ORAL	20200127	N/A	ANDA	ANDA213368	Zydus Pharmaceuticals (USA) Inc.	CHLORPROMAZINE HYDROCHLORIDE	10 mg/1	10 BLISTER PACK in 1 CARTON (70710-1129-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70710-1129-2)
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)
16714-050-01	16714-050	HUMAN PRESCRIPTION DRUG	Chlorpromazine hydrochloride	Chlorpromazine hydrochloride	TABLET, FILM COATED	ORAL	20200511	N/A	ANDA	ANDA213368	Northstar Rx LLC	CHLORPROMAZINE HYDROCHLORIDE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (16714-050-01)
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)
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)
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)
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)
70771-1509-1	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)
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)
16714-049-01	16714-049	HUMAN PRESCRIPTION DRUG	Chlorpromazine hydrochloride	Chlorpromazine hydrochloride	TABLET, FILM COATED	ORAL	20200511	N/A	ANDA	ANDA213368	Northstar Rx LLC	CHLORPROMAZINE HYDROCHLORIDE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (16714-049-01)
70771-1507-1	70771-1507	HUMAN PRESCRIPTION DRUG	Chlorpromazine hydrochloride	Chlorpromazine hydrochloride	TABLET, FILM COATED	ORAL	20200127	N/A	ANDA	ANDA213368	Zydus Lifesciences Limited	CHLORPROMAZINE HYDROCHLORIDE	25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70771-1507-1)
70771-1507-4	70771-1507	HUMAN PRESCRIPTION DRUG	Chlorpromazine hydrochloride	Chlorpromazine hydrochloride	TABLET, FILM COATED	ORAL	20200127	N/A	ANDA	ANDA213368	Zydus Lifesciences Limited	CHLORPROMAZINE HYDROCHLORIDE	25 mg/1	10 BLISTER PACK in 1 CARTON (70771-1507-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1507-2)
0904-7132-61	0904-7132	HUMAN PRESCRIPTION DRUG	Chlorpromazine hydrochloride	Chlorpromazine hydrochloride	TABLET, FILM COATED	ORAL	20200127	20260630	ANDA	ANDA213368	Major Pharmaceuticals	CHLORPROMAZINE HYDROCHLORIDE	100 mg/1	100 BLISTER PACK in 1 CARTON (0904-7132-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK
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)