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
70710-1668-1	70710-1668	HUMAN PRESCRIPTION DRUG	Prochlorperazine Maleate	Prochlorperazine Maleate	TABLET	ORAL	20220810	N/A	ANDA	ANDA216495	Zydus Pharmaceuticals (USA) Inc.	PROCHLORPERAZINE MALEATE	10 mg/1	100 TABLET in 1 BOTTLE (70710-1668-1)
70710-1667-1	70710-1667	HUMAN PRESCRIPTION DRUG	Prochlorperazine Maleate	Prochlorperazine Maleate	TABLET	ORAL	20220810	N/A	ANDA	ANDA216495	Zydus Pharmaceuticals (USA) Inc.	PROCHLORPERAZINE MALEATE	5 mg/1	100 TABLET in 1 BOTTLE (70710-1667-1)
82868-044-30	82868-044	HUMAN PRESCRIPTION DRUG	Prochlorperazine Maleate	Prochlorperazine Maleate	TABLET	ORAL	20240206	N/A	ANDA	ANDA216495	Northwind Pharmaceuticals, LLC	PROCHLORPERAZINE MALEATE	10 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (82868-044-30)
70771-1697-1	70771-1697	HUMAN PRESCRIPTION DRUG	Prochlorperazine Maleate	Prochlorperazine Maleate	TABLET	ORAL	20220810	N/A	ANDA	ANDA216495	Zydus Lifesciences Limited	PROCHLORPERAZINE MALEATE	5 mg/1	100 TABLET in 1 BOTTLE (70771-1697-1)
70771-1698-1	70771-1698	HUMAN PRESCRIPTION DRUG	Prochlorperazine Maleate	Prochlorperazine Maleate	TABLET	ORAL	20220810	N/A	ANDA	ANDA216495	Zydus Lifesciences Limited	PROCHLORPERAZINE MALEATE	10 mg/1	100 TABLET in 1 BOTTLE (70771-1698-1)