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
68382-205-10	68382-205	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET, FILM COATED	ORAL	20121016	N/A	ANDA	ANDA078926	Zydus Pharmaceuticals USA Inc.	GABAPENTIN	800 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (68382-205-10)
68382-205-77	68382-205	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET, FILM COATED	ORAL	20121016	N/A	ANDA	ANDA078926	Zydus Pharmaceuticals USA Inc.	GABAPENTIN	800 mg/1	100 BLISTER PACK in 1 CARTON (68382-205-77) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68382-205-30)
68382-204-01	68382-204	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET, FILM COATED	ORAL	20121016	N/A	ANDA	ANDA078926	Zydus Pharmaceuticals USA Inc.	GABAPENTIN	600 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68382-204-01)
68382-204-10	68382-204	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET, FILM COATED	ORAL	20121016	N/A	ANDA	ANDA078926	Zydus Pharmaceuticals USA Inc.	GABAPENTIN	600 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (68382-204-10)
68382-205-01	68382-205	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET, FILM COATED	ORAL	20121016	N/A	ANDA	ANDA078926	Zydus Pharmaceuticals USA Inc.	GABAPENTIN	800 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68382-205-01)