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
66993-345-76	66993-345	HUMAN PRESCRIPTION DRUG	Lofexidine hydrochloride	lofexidine hydrochloride	TABLET, FILM COATED	ORAL	20240829	N/A	NDA AUTHORIZED GENERIC	NDA209229	Prasco Laboratories	LOFEXIDINE HYDROCHLORIDE	.2 mg/1	1 BOTTLE in 1 CARTON (66993-345-76) / 96 TABLET, FILM COATED in 1 BOTTLE
66993-345-37	66993-345	HUMAN PRESCRIPTION DRUG	Lofexidine hydrochloride	lofexidine hydrochloride	TABLET, FILM COATED	ORAL	20240829	N/A	NDA AUTHORIZED GENERIC	NDA209229	Prasco Laboratories	LOFEXIDINE HYDROCHLORIDE	.2 mg/1	1 BOTTLE in 1 CARTON (66993-345-37) / 36 TABLET, FILM COATED in 1 BOTTLE
78670-050-36	78670-050	HUMAN PRESCRIPTION DRUG	Lucemyra	lofexidine hydrochloride	TABLET, FILM COATED	ORAL	20210209	N/A	NDA	NDA209229	USWM, LLC	LOFEXIDINE HYDROCHLORIDE	.2 mg/1	1 BOTTLE in 1 CARTON (78670-050-36) / 36 TABLET, FILM COATED in 1 BOTTLE
78670-050-03	78670-050	HUMAN PRESCRIPTION DRUG	Lucemyra	lofexidine hydrochloride	TABLET, FILM COATED	ORAL	20210209	N/A	NDA	NDA209229	USWM, LLC	LOFEXIDINE HYDROCHLORIDE	.2 mg/1	1 BOTTLE in 1 CARTON (78670-050-03) / 36 TABLET, FILM COATED in 1 BOTTLE
78670-050-96	78670-050	HUMAN PRESCRIPTION DRUG	Lucemyra	lofexidine hydrochloride	TABLET, FILM COATED	ORAL	20210209	N/A	NDA	NDA209229	USWM, LLC	LOFEXIDINE HYDROCHLORIDE	.2 mg/1	1 BOTTLE in 1 CARTON (78670-050-96) / 96 TABLET, FILM COATED in 1 BOTTLE