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
68462-889-01	68462-889	HUMAN PRESCRIPTION DRUG	PROCHLORPERAZINE MALEATE	PROCHLORPERAZINE MALEATE	TABLET	ORAL	20230317	N/A	ANDA	ANDA216595	GLENMARK PHARMACEUTICALS INC., USA	PROCHLORPERAZINE MALEATE	5 mg/1	100 TABLET in 1 BOTTLE (68462-889-01)
68462-889-10	68462-889	HUMAN PRESCRIPTION DRUG	PROCHLORPERAZINE MALEATE	PROCHLORPERAZINE MALEATE	TABLET	ORAL	20230317	N/A	ANDA	ANDA216595	GLENMARK PHARMACEUTICALS INC., USA	PROCHLORPERAZINE MALEATE	5 mg/1	1000 TABLET in 1 BOTTLE (68462-889-10)
68462-890-01	68462-890	HUMAN PRESCRIPTION DRUG	PROCHLORPERAZINE MALEATE	PROCHLORPERAZINE MALEATE	TABLET	ORAL	20230317	N/A	ANDA	ANDA216595	GLENMARK PHARMACEUTICALS INC., USA	PROCHLORPERAZINE MALEATE	10 mg/1	100 TABLET in 1 BOTTLE (68462-890-01)
68462-890-10	68462-890	HUMAN PRESCRIPTION DRUG	PROCHLORPERAZINE MALEATE	PROCHLORPERAZINE MALEATE	TABLET	ORAL	20230317	N/A	ANDA	ANDA216595	GLENMARK PHARMACEUTICALS INC., USA	PROCHLORPERAZINE MALEATE	10 mg/1	1000 TABLET in 1 BOTTLE (68462-890-10)