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
72162-1309-4	72162-1309	HUMAN PRESCRIPTION DRUG	Albendazole 200 mg	Albendazole	TABLET, FILM COATED	ORAL	20230824	N/A	ANDA	ANDA210011	Bryant Ranch Prepack	ALBENDAZOLE	200 mg/1	2 TABLET, FILM COATED in 1 BOTTLE (72162-1309-4)
42291-093-02	42291-093	HUMAN PRESCRIPTION DRUG	Albendazole 200 mg	Albendazole	TABLET, FILM COATED	ORAL	20200515	N/A	ANDA	ANDA210011	AvKARE	ALBENDAZOLE	200 mg/1	2 TABLET, FILM COATED in 1 BOTTLE (42291-093-02)
63629-9278-1	63629-9278	HUMAN PRESCRIPTION DRUG	Albendazole 200 mg	Albendazole	TABLET, FILM COATED	ORAL	20220606	N/A	ANDA	ANDA210011	Bryant Ranch Prepack	ALBENDAZOLE	200 mg/1	2 TABLET, FILM COATED in 1 BOTTLE (63629-9278-1)
63629-1221-1	63629-1221	HUMAN PRESCRIPTION DRUG	Albendazole 200 mg	Albendazole	TABLET, FILM COATED	ORAL	20210114	N/A	ANDA	ANDA210011	Bryant Ranch Prepack	ALBENDAZOLE	200 mg/1	2 TABLET, FILM COATED in 1 BOTTLE (63629-1221-1)
31722-935-28	31722-935	HUMAN PRESCRIPTION DRUG	Albendazole 200 mg	Albendazole	TABLET, FILM COATED	ORAL	20181215	N/A	ANDA	ANDA210011	Camber Pharmaceuticals	ALBENDAZOLE	200 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (31722-935-28)
31722-935-02	31722-935	HUMAN PRESCRIPTION DRUG	Albendazole 200 mg	Albendazole	TABLET, FILM COATED	ORAL	20181215	N/A	ANDA	ANDA210011	Camber Pharmaceuticals	ALBENDAZOLE	200 mg/1	2 TABLET, FILM COATED in 1 BOTTLE (31722-935-02)