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
71335-2190-4	71335-2190	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20221115	N/A	ANDA	ANDA216441	Bryant Ranch Prepack	FAMOTIDINE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-2190-4)
71335-2190-5	71335-2190	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20221115	N/A	ANDA	ANDA216441	Bryant Ranch Prepack	FAMOTIDINE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-2190-5)
71335-2190-6	71335-2190	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20221115	N/A	ANDA	ANDA216441	Bryant Ranch Prepack	FAMOTIDINE	20 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (71335-2190-6)
71335-2190-7	71335-2190	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20221115	N/A	ANDA	ANDA216441	Bryant Ranch Prepack	FAMOTIDINE	20 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-2190-7)
71335-2190-8	71335-2190	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20221115	N/A	ANDA	ANDA216441	Bryant Ranch Prepack	FAMOTIDINE	20 mg/1	50 TABLET, FILM COATED in 1 BOTTLE (71335-2190-8)
71335-2190-9	71335-2190	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20221115	N/A	ANDA	ANDA216441	Bryant Ranch Prepack	FAMOTIDINE	20 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (71335-2190-9)
68071-3521-3	68071-3521	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20231012	N/A	ANDA	ANDA216441	NuCare Pharmaceuticals,Inc.	FAMOTIDINE	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68071-3521-3)
71335-2190-3	71335-2190	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20221115	N/A	ANDA	ANDA216441	Bryant Ranch Prepack	FAMOTIDINE	20 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71335-2190-3)
71335-2190-2	71335-2190	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20221115	N/A	ANDA	ANDA216441	Bryant Ranch Prepack	FAMOTIDINE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-2190-2)
71335-2190-1	71335-2190	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20221115	N/A	ANDA	ANDA216441	Bryant Ranch Prepack	FAMOTIDINE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-2190-1)
70771-1702-0	70771-1702	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20220606	N/A	ANDA	ANDA216441	Zydus Lifesciences Limited	FAMOTIDINE	20 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (70771-1702-0)
70771-1702-5	70771-1702	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20220606	N/A	ANDA	ANDA216441	Zydus Lifesciences Limited	FAMOTIDINE	20 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (70771-1702-5)
70771-1703-0	70771-1703	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20220606	N/A	ANDA	ANDA216441	Zydus Lifesciences Limited	FAMOTIDINE	40 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (70771-1703-0)
70771-1703-1	70771-1703	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20220606	N/A	ANDA	ANDA216441	Zydus Lifesciences Limited	FAMOTIDINE	40 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70771-1703-1)
70771-1703-3	70771-1703	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20220606	N/A	ANDA	ANDA216441	Zydus Lifesciences Limited	FAMOTIDINE	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70771-1703-3)
70771-1703-4	70771-1703	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20220606	N/A	ANDA	ANDA216441	Zydus Lifesciences Limited	FAMOTIDINE	40 mg/1	10 BLISTER PACK in 1 CARTON (70771-1703-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1703-2)
70771-1703-5	70771-1703	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20220606	N/A	ANDA	ANDA216441	Zydus Lifesciences Limited	FAMOTIDINE	40 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (70771-1703-5)
60760-736-07	60760-736	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20230206	N/A	ANDA	ANDA216441	ST. MARY'S MEDICAL PARK PHARMACY	FAMOTIDINE	40 mg/1	7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-736-07)
60760-736-60	60760-736	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20221208	N/A	ANDA	ANDA216441	ST. MARY'S MEDICAL PARK PHARMACY	FAMOTIDINE	40 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-736-60)
70771-1702-1	70771-1702	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20220606	N/A	ANDA	ANDA216441	Zydus Lifesciences Limited	FAMOTIDINE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70771-1702-1)