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
16714-122-01	16714-122	HUMAN PRESCRIPTION DRUG	Pilocarpine Hydrochloride	pilocarpine hydrochloride	TABLET, FILM COATED	ORAL	20190813	N/A	ANDA	ANDA212377	NorthStar Rx LLC	PILOCARPINE HYDROCHLORIDE	7.5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (16714-122-01)
16714-121-01	16714-121	HUMAN PRESCRIPTION DRUG	Pilocarpine Hydrochloride	pilocarpine hydrochloride	TABLET, FILM COATED	ORAL	20190813	N/A	ANDA	ANDA212377	NorthStar Rx LLC	PILOCARPINE HYDROCHLORIDE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (16714-121-01)
59651-225-01	59651-225	HUMAN PRESCRIPTION DRUG	Pilocarpine Hydrochloride	pilocarpine hydrochloride	TABLET, FILM COATED	ORAL	20190813	N/A	ANDA	ANDA212377	Aurobindo Pharma Limited	PILOCARPINE HYDROCHLORIDE	7.5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (59651-225-01)
59651-224-01	59651-224	HUMAN PRESCRIPTION DRUG	Pilocarpine Hydrochloride	pilocarpine hydrochloride	TABLET, FILM COATED	ORAL	20190813	N/A	ANDA	ANDA212377	Aurobindo Pharma Limited	PILOCARPINE HYDROCHLORIDE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (59651-224-01)
71335-2094-1	71335-2094	HUMAN PRESCRIPTION DRUG	Pilocarpine Hydrochloride	pilocarpine hydrochloride	TABLET, FILM COATED	ORAL	20220523	N/A	ANDA	ANDA212377	Bryant Ranch Prepack	PILOCARPINE HYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-2094-1)