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
69844-038-01	69844-038	HUMAN PRESCRIPTION DRUG	DONEPEZIL HYDROCHLORIDE	DONEPEZIL HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20200406	N/A	ANDA	ANDA202114	Graviti Pharmaceuticals Private Limited	DONEPEZIL HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (69844-038-01)
69844-038-02	69844-038	HUMAN PRESCRIPTION DRUG	DONEPEZIL HYDROCHLORIDE	DONEPEZIL HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20200406	N/A	ANDA	ANDA202114	Graviti Pharmaceuticals Private Limited	DONEPEZIL HYDROCHLORIDE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (69844-038-02)
69844-038-03	69844-038	HUMAN PRESCRIPTION DRUG	DONEPEZIL HYDROCHLORIDE	DONEPEZIL HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20200406	N/A	ANDA	ANDA202114	Graviti Pharmaceuticals Private Limited	DONEPEZIL HYDROCHLORIDE	10 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (69844-038-03)
69844-037-01	69844-037	HUMAN PRESCRIPTION DRUG	DONEPEZIL HYDROCHLORIDE	DONEPEZIL HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20200406	N/A	ANDA	ANDA202114	Graviti Pharmaceuticals Private Limited	DONEPEZIL HYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (69844-037-01)
69844-037-02	69844-037	HUMAN PRESCRIPTION DRUG	DONEPEZIL HYDROCHLORIDE	DONEPEZIL HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20200406	N/A	ANDA	ANDA202114	Graviti Pharmaceuticals Private Limited	DONEPEZIL HYDROCHLORIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (69844-037-02)
69844-037-03	69844-037	HUMAN PRESCRIPTION DRUG	DONEPEZIL HYDROCHLORIDE	DONEPEZIL HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20200406	N/A	ANDA	ANDA202114	Graviti Pharmaceuticals Private Limited	DONEPEZIL HYDROCHLORIDE	5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (69844-037-03)