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
31722-036-01	31722-036	HUMAN PRESCRIPTION DRUG	Mexiletine hydrochloride	Mexiletine hydrochloride	CAPSULE	ORAL	20221109	N/A	ANDA	ANDA216463	Camber Pharmaceuticals, Inc.	MEXILETINE HYDROCHLORIDE	150 mg/1	100 CAPSULE in 1 BOTTLE (31722-036-01)
31722-038-01	31722-038	HUMAN PRESCRIPTION DRUG	Mexiletine hydrochloride	Mexiletine hydrochloride	CAPSULE	ORAL	20221109	N/A	ANDA	ANDA216463	Camber Pharmaceuticals, Inc.	MEXILETINE HYDROCHLORIDE	250 mg/1	100 CAPSULE in 1 BOTTLE (31722-038-01)
31722-037-01	31722-037	HUMAN PRESCRIPTION DRUG	Mexiletine hydrochloride	Mexiletine hydrochloride	CAPSULE	ORAL	20221109	N/A	ANDA	ANDA216463	Camber Pharmaceuticals, Inc.	MEXILETINE HYDROCHLORIDE	200 mg/1	100 CAPSULE in 1 BOTTLE (31722-037-01)
60687-778-21	60687-778	HUMAN PRESCRIPTION DRUG	Mexiletine hydrochloride	Mexiletine hydrochloride	CAPSULE	ORAL	20240223	N/A	ANDA	ANDA216463	American Health Packaging	MEXILETINE HYDROCHLORIDE	150 mg/1	30 BLISTER PACK in 1 CARTON (60687-778-21) / 1 CAPSULE in 1 BLISTER PACK (60687-778-11)