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
71209-020-01	71209-020	HUMAN PRESCRIPTION DRUG	DONEPEZIL HYDROCHLORIDE	donepezil hydrochloride	TABLET, FILM COATED	ORAL	20181124	N/A	ANDA	ANDA204609	Cadila Pharmaceuticals Limited	DONEPEZIL HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71209-020-01)
71209-020-04	71209-020	HUMAN PRESCRIPTION DRUG	DONEPEZIL HYDROCHLORIDE	donepezil hydrochloride	TABLET, FILM COATED	ORAL	20181124	N/A	ANDA	ANDA204609	Cadila Pharmaceuticals Limited	DONEPEZIL HYDROCHLORIDE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71209-020-04)
71209-020-11	71209-020	HUMAN PRESCRIPTION DRUG	DONEPEZIL HYDROCHLORIDE	donepezil hydrochloride	TABLET, FILM COATED	ORAL	20181124	N/A	ANDA	ANDA204609	Cadila Pharmaceuticals Limited	DONEPEZIL HYDROCHLORIDE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (71209-020-11)
71209-019-11	71209-019	HUMAN PRESCRIPTION DRUG	DONEPEZIL HYDROCHLORIDE	donepezil hydrochloride	TABLET, FILM COATED	ORAL	20181124	N/A	ANDA	ANDA204609	Cadila Pharmaceuticals Limited	DONEPEZIL HYDROCHLORIDE	5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (71209-019-11)
71209-019-04	71209-019	HUMAN PRESCRIPTION DRUG	DONEPEZIL HYDROCHLORIDE	donepezil hydrochloride	TABLET, FILM COATED	ORAL	20181124	N/A	ANDA	ANDA204609	Cadila Pharmaceuticals Limited	DONEPEZIL HYDROCHLORIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71209-019-04)
71209-019-01	71209-019	HUMAN PRESCRIPTION DRUG	DONEPEZIL HYDROCHLORIDE	donepezil hydrochloride	TABLET, FILM COATED	ORAL	20181124	N/A	ANDA	ANDA204609	Cadila Pharmaceuticals Limited	DONEPEZIL HYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71209-019-01)