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
63187-231-78	63187-231	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20181201	N/A	ANDA	ANDA202764	Proficient Rx LP	GABAPENTIN	800 mg/1	180 TABLET in 1 BOTTLE (63187-231-78)
63187-231-90	63187-231	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20181201	N/A	ANDA	ANDA202764	Proficient Rx LP	GABAPENTIN	800 mg/1	90 TABLET in 1 BOTTLE (63187-231-90)
69097-811-02	69097-811	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20160722	N/A	ANDA	ANDA202764	Cipla USA Inc.	GABAPENTIN	800 mg/1	30 TABLET in 1 BOTTLE (69097-811-02)
69097-811-07	69097-811	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20160722	N/A	ANDA	ANDA202764	Cipla USA Inc.	GABAPENTIN	800 mg/1	100 TABLET in 1 BOTTLE (69097-811-07)
69097-811-12	69097-811	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20160722	N/A	ANDA	ANDA202764	Cipla USA Inc.	GABAPENTIN	800 mg/1	500 TABLET in 1 BOTTLE (69097-811-12)
69097-812-02	69097-812	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20160722	N/A	ANDA	ANDA202764	Cipla USA Inc.	GABAPENTIN	600 mg/1	30 TABLET in 1 BOTTLE (69097-812-02)
69097-812-07	69097-812	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20160722	N/A	ANDA	ANDA202764	Cipla USA Inc.	GABAPENTIN	600 mg/1	100 TABLET in 1 BOTTLE (69097-812-07)
69097-812-12	69097-812	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20160722	N/A	ANDA	ANDA202764	Cipla USA Inc.	GABAPENTIN	600 mg/1	500 TABLET in 1 BOTTLE (69097-812-12)
63187-785-00	63187-785	HUMAN PRESCRIPTION DRUG	Gabapentin	Gabapentin	TABLET	ORAL	20161201	N/A	ANDA	ANDA202764	Proficient Rx LP	GABAPENTIN	600 mg/1	100 TABLET in 1 BOTTLE (63187-785-00)