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
65862-860-01	65862-860	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20151222	N/A	ANDA	ANDA206530	Aurobindo Pharma Limited	FAMOTIDINE	40 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65862-860-01)
65862-860-05	65862-860	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20151222	N/A	ANDA	ANDA206530	Aurobindo Pharma Limited	FAMOTIDINE	40 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65862-860-05)
65862-860-30	65862-860	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20151222	N/A	ANDA	ANDA206530	Aurobindo Pharma Limited	FAMOTIDINE	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65862-860-30)
65862-860-78	65862-860	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20151222	N/A	ANDA	ANDA206530	Aurobindo Pharma Limited	FAMOTIDINE	40 mg/1	10 BLISTER PACK in 1 CARTON (65862-860-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-860-10)
65862-860-99	65862-860	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20151222	N/A	ANDA	ANDA206530	Aurobindo Pharma Limited	FAMOTIDINE	40 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65862-860-99)
50090-6916-0	50090-6916	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20231213	N/A	ANDA	ANDA206530	A-S Medication Solutions	FAMOTIDINE	40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-6916-0)
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)
60687-595-01	60687-595	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20210309	N/A	ANDA	ANDA206530	American Health Packaging	FAMOTIDINE	20 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-595-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-595-11)
65862-859-01	65862-859	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20151222	N/A	ANDA	ANDA206530	Aurobindo Pharma Limited	FAMOTIDINE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65862-859-01)
65862-859-05	65862-859	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20151222	N/A	ANDA	ANDA206530	Aurobindo Pharma Limited	FAMOTIDINE	20 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65862-859-05)
65862-859-30	65862-859	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20151222	N/A	ANDA	ANDA206530	Aurobindo Pharma Limited	FAMOTIDINE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65862-859-30)
65862-859-78	65862-859	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20151222	N/A	ANDA	ANDA206530	Aurobindo Pharma Limited	FAMOTIDINE	20 mg/1	10 BLISTER PACK in 1 CARTON (65862-859-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-859-10)
65862-859-99	65862-859	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20151222	N/A	ANDA	ANDA206530	Aurobindo Pharma Limited	FAMOTIDINE	20 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65862-859-99)
67296-1795-3	67296-1795	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20190619	N/A	ANDA	ANDA206530	RedPharm Drug, Inc.	FAMOTIDINE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (67296-1795-3)