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
33342-555-11	33342-555	HUMAN PRESCRIPTION DRUG	Mexiletine Hydrochloride	Mexiletine Hydrochloride	CAPSULE	ORAL	20260323	N/A	ANDA	ANDA219987	Macleods Pharmaceuticals Limited	MEXILETINE HYDROCHLORIDE	150 mg/1	100 CAPSULE in 1 CONTAINER (33342-555-11)
33342-555-12	33342-555	HUMAN PRESCRIPTION DRUG	Mexiletine Hydrochloride	Mexiletine Hydrochloride	CAPSULE	ORAL	20260323	N/A	ANDA	ANDA219987	Macleods Pharmaceuticals Limited	MEXILETINE HYDROCHLORIDE	150 mg/1	10 BLISTER PACK in 1 CARTON (33342-555-12) / 10 CAPSULE in 1 BLISTER PACK
33342-556-11	33342-556	HUMAN PRESCRIPTION DRUG	Mexiletine Hydrochloride	Mexiletine Hydrochloride	CAPSULE	ORAL	20260323	N/A	ANDA	ANDA219987	Macleods Pharmaceuticals Limited	MEXILETINE HYDROCHLORIDE	200 mg/1	100 CAPSULE in 1 CONTAINER (33342-556-11)
33342-556-12	33342-556	HUMAN PRESCRIPTION DRUG	Mexiletine Hydrochloride	Mexiletine Hydrochloride	CAPSULE	ORAL	20260323	N/A	ANDA	ANDA219987	Macleods Pharmaceuticals Limited	MEXILETINE HYDROCHLORIDE	200 mg/1	10 BLISTER PACK in 1 CARTON (33342-556-12) / 10 CAPSULE in 1 BLISTER PACK
33342-557-11	33342-557	HUMAN PRESCRIPTION DRUG	Mexiletine Hydrochloride	Mexiletine Hydrochloride	CAPSULE	ORAL	20260323	N/A	ANDA	ANDA219987	Macleods Pharmaceuticals Limited	MEXILETINE HYDROCHLORIDE	200 mg/1	100 CAPSULE in 1 CONTAINER (33342-557-11)
33342-557-12	33342-557	HUMAN PRESCRIPTION DRUG	Mexiletine Hydrochloride	Mexiletine Hydrochloride	CAPSULE	ORAL	20260323	N/A	ANDA	ANDA219987	Macleods Pharmaceuticals Limited	MEXILETINE HYDROCHLORIDE	200 mg/1	10 BLISTER PACK in 1 CARTON (33342-557-12) / 10 CAPSULE in 1 BLISTER PACK