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
68084-928-25	68084-928	HUMAN PRESCRIPTION DRUG	Pilocarpine hydrochloride	Pilocarpine hydrochloride	TABLET, FILM COATED	ORAL	20150925	N/A	NDA AUTHORIZED GENERIC	NDA020237	American Health Packaging	PILOCARPINE HYDROCHLORIDE	5 mg/1	30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-928-25) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-928-95)
59212-775-10	59212-775	HUMAN PRESCRIPTION DRUG	Salagen	Pilocarpine Hydrochloride	TABLET, FILM COATED	ORAL	20190901	N/A	NDA	NDA020237	Advanz Pharma (US) Corp.	PILOCARPINE HYDROCHLORIDE	7.5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (59212-775-10)
0228-2801-11	0228-2801	HUMAN PRESCRIPTION DRUG	Pilocarpine hydrochloride	Pilocarpine hydrochloride	TABLET, FILM COATED	ORAL	20110913	N/A	NDA AUTHORIZED GENERIC	NDA020237	Actavis Pharma, Inc.	PILOCARPINE HYDROCHLORIDE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0228-2801-11)
59212-705-10	59212-705	HUMAN PRESCRIPTION DRUG	Salagen	Pilocarpine Hydrochloride	TABLET, FILM COATED	ORAL	20190901	N/A	NDA	NDA020237	Advanz Pharma (US) Corp.	PILOCARPINE HYDROCHLORIDE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (59212-705-10)
0228-2837-11	0228-2837	HUMAN PRESCRIPTION DRUG	Pilocarpine hydrochloride	Pilocarpine hydrochloride	TABLET, FILM COATED	ORAL	20110913	N/A	NDA AUTHORIZED GENERIC	NDA020237	Actavis Pharma, Inc.	PILOCARPINE HYDROCHLORIDE	7.5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0228-2837-11)