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
63629-8351-1	63629-8351	HUMAN PRESCRIPTION DRUG	Pilocarpine Hydrochloride	Pilocarpine Hydrochloride	TABLET, FILM COATED	ORAL	20200902	N/A	ANDA	ANDA077220	Bryant Ranch Prepack	PILOCARPINE HYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63629-8351-1)
72162-1078-1	72162-1078	HUMAN PRESCRIPTION DRUG	Pilocarpine Hydrochloride	Pilocarpine Hydrochloride	TABLET, FILM COATED	ORAL	20230830	N/A	ANDA	ANDA077220	Bryant Ranch Prepack	PILOCARPINE HYDROCHLORIDE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (72162-1078-1)
0527-1407-01	0527-1407	HUMAN PRESCRIPTION DRUG	Pilocarpine Hydrochloride	Pilocarpine Hydrochloride	TABLET, FILM COATED	ORAL	20051014	N/A	ANDA	ANDA077220	Lannett Company, Inc.	PILOCARPINE HYDROCHLORIDE	7.5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (0527-1407-01)
63629-2099-1	63629-2099	HUMAN PRESCRIPTION DRUG	Pilocarpine Hydrochloride	Pilocarpine Hydrochloride	TABLET, FILM COATED	ORAL	20210129	N/A	ANDA	ANDA077220	Bryant Ranch Prepack	PILOCARPINE HYDROCHLORIDE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (63629-2099-1)
0527-1313-01	0527-1313	HUMAN PRESCRIPTION DRUG	Pilocarpine Hydrochloride	Pilocarpine Hydrochloride	TABLET, FILM COATED	ORAL	20051014	N/A	ANDA	ANDA077220	Lannett Company, Inc.	PILOCARPINE HYDROCHLORIDE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (0527-1313-01)
50268-652-12	50268-652	HUMAN PRESCRIPTION DRUG	Pilocarpine Hydrochloride	Pilocarpine Hydrochloride	TABLET, FILM COATED	ORAL	20210107	N/A	ANDA	ANDA077220	AvPAK	PILOCARPINE HYDROCHLORIDE	5 mg/1	20 BLISTER PACK in 1 BOX (50268-652-12) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-652-11)