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
70518-3829-1	70518-3829	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20231106	N/A	ANDA	ANDA215630	REMEDYREPACK INC.	FAMOTIDINE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3829-1)
70518-3829-3	70518-3829	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20240124	N/A	ANDA	ANDA215630	REMEDYREPACK INC.	FAMOTIDINE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3829-3)
70518-3829-4	70518-3829	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20240228	N/A	ANDA	ANDA215630	REMEDYREPACK INC.	FAMOTIDINE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3829-4)
70518-3829-5	70518-3829	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20240612	N/A	ANDA	ANDA215630	REMEDYREPACK INC.	FAMOTIDINE	20 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3829-5)
70518-3829-6	70518-3829	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20241121	N/A	ANDA	ANDA215630	REMEDYREPACK INC.	FAMOTIDINE	20 mg/1	14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3829-6)
70518-3829-7	70518-3829	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20250104	N/A	ANDA	ANDA215630	REMEDYREPACK INC.	FAMOTIDINE	20 mg/1	60 TABLET, FILM COATED in 1 BLISTER PACK (70518-3829-7)
70518-3829-8	70518-3829	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20250114	N/A	ANDA	ANDA215630	REMEDYREPACK INC.	FAMOTIDINE	20 mg/1	14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3829-8)
70518-3829-9	70518-3829	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20251015	N/A	ANDA	ANDA215630	REMEDYREPACK INC.	FAMOTIDINE	20 mg/1	25 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3829-9)
70518-4084-1	70518-4084	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20250529	N/A	ANDA	ANDA215630	REMEDYREPACK INC.	FAMOTIDINE	40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4084-1)
70518-4084-2	70518-4084	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20251012	N/A	ANDA	ANDA215630	REMEDYREPACK INC.	FAMOTIDINE	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4084-2)
68071-3413-3	68071-3413	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20230523	N/A	ANDA	ANDA215630	NuCare Pharmceuticals,Inc.	FAMOTIDINE	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68071-3413-3)
68071-3420-3	68071-3420	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20230726	N/A	ANDA	ANDA215630	NuCare Pharmaceuticals,Inc.	FAMOTIDINE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68071-3420-3)
68071-3420-6	68071-3420	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20230601	N/A	ANDA	ANDA215630	NuCare Pharmaceuticals,Inc.	FAMOTIDINE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68071-3420-6)
68071-3420-7	68071-3420	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20230726	N/A	ANDA	ANDA215630	NuCare Pharmaceuticals,Inc.	FAMOTIDINE	20 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (68071-3420-7)
68071-3420-8	68071-3420	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20230726	N/A	ANDA	ANDA215630	NuCare Pharmaceuticals,Inc.	FAMOTIDINE	20 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (68071-3420-8)
68071-3420-9	68071-3420	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20230726	N/A	ANDA	ANDA215630	NuCare Pharmaceuticals,Inc.	FAMOTIDINE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68071-3420-9)
76420-712-01	76420-712	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20240411	N/A	ANDA	ANDA215630	Asclemed USA, Inc.	FAMOTIDINE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (76420-712-01)
76420-712-30	76420-712	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20240411	N/A	ANDA	ANDA215630	Asclemed USA, Inc.	FAMOTIDINE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (76420-712-30)
76420-712-60	76420-712	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20240411	N/A	ANDA	ANDA215630	Asclemed USA, Inc.	FAMOTIDINE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (76420-712-60)
76420-712-90	76420-712	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20240411	N/A	ANDA	ANDA215630	Asclemed USA, Inc.	FAMOTIDINE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (76420-712-90)