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
72789-517-01	72789-517	HUMAN PRESCRIPTION DRUG	PROCHLORPERAZINE MALEATE	PROCHLORPERAZINE MALEATE	TABLET, FILM COATED	ORAL	20250728	N/A	ANDA	ANDA218912	PD-Rx Pharmaceuticals, Inc.	PROCHLORPERAZINE MALEATE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-517-01)
72789-517-90	72789-517	HUMAN PRESCRIPTION DRUG	PROCHLORPERAZINE MALEATE	PROCHLORPERAZINE MALEATE	TABLET, FILM COATED	ORAL	20250728	N/A	ANDA	ANDA218912	PD-Rx Pharmaceuticals, Inc.	PROCHLORPERAZINE MALEATE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-517-90)
72789-518-90	72789-518	HUMAN PRESCRIPTION DRUG	PROCHLORPERAZINE MALEATE	PROCHLORPERAZINE MALEATE	TABLET, FILM COATED	ORAL	20250728	N/A	ANDA	ANDA218912	PD-Rx Pharmaceuticals, Inc.	PROCHLORPERAZINE MALEATE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-518-90)
72789-518-01	72789-518	HUMAN PRESCRIPTION DRUG	PROCHLORPERAZINE MALEATE	PROCHLORPERAZINE MALEATE	TABLET, FILM COATED	ORAL	20250728	N/A	ANDA	ANDA218912	PD-Rx Pharmaceuticals, Inc.	PROCHLORPERAZINE MALEATE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-518-01)
69315-265-01	69315-265	HUMAN PRESCRIPTION DRUG	PROCHLORPERAZINE MALEATE	PROCHLORPERAZINE MALEATE	TABLET, FILM COATED	ORAL	20250625	N/A	ANDA	ANDA218912	Leading Pharma, LLC	PROCHLORPERAZINE MALEATE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (69315-265-01)
69315-266-01	69315-266	HUMAN PRESCRIPTION DRUG	PROCHLORPERAZINE MALEATE	PROCHLORPERAZINE MALEATE	TABLET, FILM COATED	ORAL	20250625	N/A	ANDA	ANDA218912	Leading Pharma, LLC	PROCHLORPERAZINE MALEATE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (69315-266-01)