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
60219-2038-1	60219-2038	HUMAN PRESCRIPTION DRUG	prochlorperazine maleate	prochlorperazine maleate	TABLET, FILM COATED	ORAL	20230421	N/A	ANDA	ANDA216598	Amneal Pharmaceuticals NY LLC	PROCHLORPERAZINE MALEATE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60219-2038-1)
60219-2038-7	60219-2038	HUMAN PRESCRIPTION DRUG	prochlorperazine maleate	prochlorperazine maleate	TABLET, FILM COATED	ORAL	20230421	N/A	ANDA	ANDA216598	Amneal Pharmaceuticals NY LLC	PROCHLORPERAZINE MALEATE	5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60219-2038-7)
60219-2039-1	60219-2039	HUMAN PRESCRIPTION DRUG	prochlorperazine maleate	prochlorperazine maleate	TABLET, FILM COATED	ORAL	20230421	N/A	ANDA	ANDA216598	Amneal Pharmaceuticals NY LLC	PROCHLORPERAZINE MALEATE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60219-2039-1)
60219-2039-7	60219-2039	HUMAN PRESCRIPTION DRUG	prochlorperazine maleate	prochlorperazine maleate	TABLET, FILM COATED	ORAL	20230421	N/A	ANDA	ANDA216598	Amneal Pharmaceuticals NY LLC	PROCHLORPERAZINE MALEATE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60219-2039-7)