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
16837-872-75	16837-872	HUMAN OTC DRUG	Pepcid AC Original Strength	Famotidine	TABLET, FILM COATED	ORAL	20210315	20240831	NDA	NDA020325	Johnson & Johnson Consumer Inc.	FAMOTIDINE	10 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (16837-872-75) / 75 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
16837-872-90	16837-872	HUMAN OTC DRUG	Pepcid AC Original Strength	Famotidine	TABLET, FILM COATED	ORAL	19951001	N/A	NDA	NDA020325	Johnson & Johnson Consumer Inc.	FAMOTIDINE	10 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (16837-872-90) / 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
16837-889-20	16837-889	HUMAN OTC DRUG	Maximum Strength PEPCID AC Icy Cool Mint	Famotidine	TABLET, FILM COATED	ORAL	20240311	N/A	NDA	NDA020325	Johnson & Johnson Consumer Inc.	FAMOTIDINE	20 mg/1	1 BOTTLE in 1 CARTON (16837-889-20) / 20 TABLET, FILM COATED in 1 BOTTLE
16837-889-40	16837-889	HUMAN OTC DRUG	Maximum Strength PEPCID AC Icy Cool Mint	Famotidine	TABLET, FILM COATED	ORAL	20240311	N/A	NDA	NDA020325	Johnson & Johnson Consumer Inc.	FAMOTIDINE	20 mg/1	1 BOTTLE in 1 CARTON (16837-889-40) / 40 TABLET, FILM COATED in 1 BOTTLE
16837-855-09	16837-855	HUMAN OTC DRUG	PEPCID AC Maximum Strength	Famotidine	TABLET, FILM COATED	ORAL	20030901	N/A	NDA	NDA020325	Johnson & Johnson Consumer Inc.	FAMOTIDINE	20 mg/1	1 BOTTLE, PLASTIC in 1 PACKAGE (16837-855-09) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
16837-855-12	16837-855	HUMAN OTC DRUG	PEPCID AC Maximum Strength	Famotidine	TABLET, FILM COATED	ORAL	20030901	N/A	NDA	NDA020325	Johnson & Johnson Consumer Inc.	FAMOTIDINE	20 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (16837-855-12) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
16837-855-13	16837-855	HUMAN OTC DRUG	PEPCID AC Maximum Strength	Famotidine	TABLET, FILM COATED	ORAL	20030901	N/A	NDA	NDA020325	Johnson & Johnson Consumer Inc.	FAMOTIDINE	20 mg/1	1 TABLET, FILM COATED in 1 POUCH (16837-855-13)