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
71335-0370-5	71335-0370	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20211227	N/A	ANDA	ANDA206530	Bryant Ranch Prepack	FAMOTIDINE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-0370-5)
71335-0370-6	71335-0370	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20210629	N/A	ANDA	ANDA206530	Bryant Ranch Prepack	FAMOTIDINE	20 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (71335-0370-6)
71335-0370-7	71335-0370	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20210902	N/A	ANDA	ANDA206530	Bryant Ranch Prepack	FAMOTIDINE	20 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-0370-7)
68001-397-00	68001-397	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20190619	N/A	ANDA	ANDA206530	BluePoint Laboratories	FAMOTIDINE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68001-397-00)
68001-397-08	68001-397	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20190619	N/A	ANDA	ANDA206530	BluePoint Laboratories	FAMOTIDINE	20 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (68001-397-08)
68001-398-00	68001-398	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20190619	N/A	ANDA	ANDA206530	BluePoint Laboratories	FAMOTIDINE	40 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68001-398-00)
68001-398-03	68001-398	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20190619	N/A	ANDA	ANDA206530	BluePoint Laboratories	FAMOTIDINE	40 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (68001-398-03)
71205-535-06	71205-535	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20210224	N/A	ANDA	ANDA206530	Proficient Rx LP	FAMOTIDINE	20 mg/1	6 TABLET, FILM COATED in 1 BOTTLE (71205-535-06)
71205-535-78	71205-535	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20240906	N/A	ANDA	ANDA206530	Proficient Rx LP	FAMOTIDINE	20 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (71205-535-78)
71205-535-10	71205-535	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20210224	N/A	ANDA	ANDA206530	Proficient Rx LP	FAMOTIDINE	20 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (71205-535-10)
71205-535-30	71205-535	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20210216	N/A	ANDA	ANDA206530	Proficient Rx LP	FAMOTIDINE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71205-535-30)
71205-535-60	71205-535	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20210216	N/A	ANDA	ANDA206530	Proficient Rx LP	FAMOTIDINE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71205-535-60)