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
70710-1021-6	70710-1021	HUMAN PRESCRIPTION DRUG	Albendazole	Albendazole	TABLET, FILM COATED	ORAL	20200511	N/A	ANDA	ANDA208979	Zydus Pharmaceuticals USA Inc.	ALBENDAZOLE	200 mg/1	2 TABLET, FILM COATED in 1 BOTTLE (70710-1021-6)
70710-1021-7	70710-1021	HUMAN PRESCRIPTION DRUG	Albendazole	Albendazole	TABLET, FILM COATED	ORAL	20181217	N/A	ANDA	ANDA208979	Zydus Pharmaceuticals USA Inc.	ALBENDAZOLE	200 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (70710-1021-7)
70710-1021-8	70710-1021	HUMAN PRESCRIPTION DRUG	Albendazole	Albendazole	TABLET, FILM COATED	ORAL	20181217	N/A	ANDA	ANDA208979	Zydus Pharmaceuticals USA Inc.	ALBENDAZOLE	200 mg/1	1 BLISTER PACK in 1 BOTTLE (70710-1021-8) / 2 TABLET, FILM COATED in 1 BLISTER PACK
70710-1021-5	70710-1021	HUMAN PRESCRIPTION DRUG	Albendazole	Albendazole	TABLET, FILM COATED	ORAL	20181217	N/A	ANDA	ANDA208979	Zydus Pharmaceuticals USA Inc.	ALBENDAZOLE	200 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (70710-1021-5)
70710-1021-3	70710-1021	HUMAN PRESCRIPTION DRUG	Albendazole	Albendazole	TABLET, FILM COATED	ORAL	20200527	N/A	ANDA	ANDA208979	Zydus Pharmaceuticals USA Inc.	ALBENDAZOLE	200 mg/1	1 BLISTER PACK in 1 CARTON (70710-1021-3) / 2 TABLET, FILM COATED in 1 BLISTER PACK
70710-1021-1	70710-1021	HUMAN PRESCRIPTION DRUG	Albendazole	Albendazole	TABLET, FILM COATED	ORAL	20181217	N/A	ANDA	ANDA208979	Zydus Pharmaceuticals USA Inc.	ALBENDAZOLE	200 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70710-1021-1)
70771-1103-1	70771-1103	HUMAN PRESCRIPTION DRUG	Albendazole	Albendazole	TABLET, FILM COATED	ORAL	20181217	N/A	ANDA	ANDA208979	Zydus Lifesciences Limited	ALBENDAZOLE	200 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70771-1103-1)
70771-1103-7	70771-1103	HUMAN PRESCRIPTION DRUG	Albendazole	Albendazole	TABLET, FILM COATED	ORAL	20181217	N/A	ANDA	ANDA208979	Zydus Lifesciences Limited	ALBENDAZOLE	200 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (70771-1103-7)
70771-1103-3	70771-1103	HUMAN PRESCRIPTION DRUG	Albendazole	Albendazole	TABLET, FILM COATED	ORAL	20200527	N/A	ANDA	ANDA208979	Zydus Lifesciences Limited	ALBENDAZOLE	200 mg/1	1 BLISTER PACK in 1 CARTON (70771-1103-3) / 2 TABLET, FILM COATED in 1 BLISTER PACK
70771-1103-5	70771-1103	HUMAN PRESCRIPTION DRUG	Albendazole	Albendazole	TABLET, FILM COATED	ORAL	20181217	N/A	ANDA	ANDA208979	Zydus Lifesciences Limited	ALBENDAZOLE	200 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (70771-1103-5)
70771-1103-6	70771-1103	HUMAN PRESCRIPTION DRUG	Albendazole	Albendazole	TABLET, FILM COATED	ORAL	20200511	N/A	ANDA	ANDA208979	Zydus Lifesciences Limited	ALBENDAZOLE	200 mg/1	2 TABLET, FILM COATED in 1 BOTTLE (70771-1103-6)
70771-1103-8	70771-1103	HUMAN PRESCRIPTION DRUG	Albendazole	Albendazole	TABLET, FILM COATED	ORAL	20181217	N/A	ANDA	ANDA208979	Zydus Lifesciences Limited	ALBENDAZOLE	200 mg/1	1 BLISTER PACK in 1 BOTTLE (70771-1103-8) / 2 TABLET, FILM COATED in 1 BLISTER PACK