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
0904-7382-06	0904-7382	HUMAN PRESCRIPTION DRUG	Prochlorperazine Maleate	Prochlorperazine Maleate	TABLET	ORAL	20231030	N/A	ANDA	ANDA216202	Major Pharmaceuticals	PROCHLORPERAZINE MALEATE	10 mg/1	50 BLISTER PACK in 1 CARTON (0904-7382-06) / 1 TABLET in 1 BLISTER PACK
0904-7381-06	0904-7381	HUMAN PRESCRIPTION DRUG	Prochlorperazine Maleate	Prochlorperazine Maleate	TABLET	ORAL	20231030	N/A	ANDA	ANDA216202	Major Pharmaceuticals	PROCHLORPERAZINE MALEATE	5 mg/1	50 BLISTER PACK in 1 CARTON (0904-7381-06) / 1 TABLET in 1 BLISTER PACK
72603-169-01	72603-169	HUMAN PRESCRIPTION DRUG	Prochlorperazine Maleate	Prochlorperazine Maleate	TABLET	ORAL	20230907	N/A	ANDA	ANDA216202	Northstar Rx LLC	PROCHLORPERAZINE MALEATE	10 mg/1	100 TABLET in 1 BOTTLE (72603-169-01)
72603-168-01	72603-168	HUMAN PRESCRIPTION DRUG	Prochlorperazine Maleate	Prochlorperazine Maleate	TABLET	ORAL	20230907	N/A	ANDA	ANDA216202	Northstar Rx LLC	PROCHLORPERAZINE MALEATE	5 mg/1	100 TABLET in 1 BOTTLE (72603-168-01)
70954-688-10	70954-688	HUMAN PRESCRIPTION DRUG	Prochlorperazine Maleate	Prochlorperazine Maleate	TABLET	ORAL	20220801	N/A	ANDA	ANDA216202	ANI Pharmaceuticals, Inc.	PROCHLORPERAZINE MALEATE	5 mg/1	100 TABLET in 1 BOTTLE (70954-688-10)
70954-689-10	70954-689	HUMAN PRESCRIPTION DRUG	Prochlorperazine Maleate	Prochlorperazine Maleate	TABLET	ORAL	20220801	N/A	ANDA	ANDA216202	ANI Pharmaceuticals, Inc.	PROCHLORPERAZINE MALEATE	10 mg/1	100 TABLET in 1 BOTTLE (70954-689-10)