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）
检索条件:" 注册申请号=ANDA200651"
符合检索条件的记录共 70 条，共 4 页，当前第 3 页 ，可点击列名称排序
首页 上一页 下一页 最后一页
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
82009-071-05 82009-071 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET, FILM COATED ORAL 20230901 N/A ANDA ANDA200651 QUALLENT PHARMACEUTICALS HEALTH LLC GABAPENTIN 600 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (82009-071-05)
82009-072-05 82009-072 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET, FILM COATED ORAL 20230901 N/A ANDA ANDA200651 QUALLENT PHARMACEUTICALS HEALTH LLC GABAPENTIN 800 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (82009-072-05)
72189-092-90 72189-092 HUMAN PRESCRIPTION DRUG GABAPENTIN GABAPENTIN TABLET, FILM COATED ORAL 20200515 N/A ANDA ANDA200651 DIRECT RX GABAPENTIN 800 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (72189-092-90)
16714-330-01 16714-330 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET, FILM COATED ORAL 20111006 N/A ANDA ANDA200651 NorthStar Rx LLC GABAPENTIN 600 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (16714-330-01)
16714-330-02 16714-330 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET, FILM COATED ORAL 20111006 N/A ANDA ANDA200651 NorthStar Rx LLC GABAPENTIN 600 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (16714-330-02)
16714-332-01 16714-332 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET, FILM COATED ORAL 20111006 N/A ANDA ANDA200651 NorthStar Rx LLC GABAPENTIN 800 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (16714-332-01)
16714-332-02 16714-332 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET, FILM COATED ORAL 20111006 N/A ANDA ANDA200651 NorthStar Rx LLC GABAPENTIN 800 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (16714-332-02)
70518-2323-0 70518-2323 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET, FILM COATED ORAL 20190924 N/A ANDA ANDA200651 REMEDYREPACK INC. GABAPENTIN 800 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2323-0)
70518-2323-1 70518-2323 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET, FILM COATED ORAL 20191004 N/A ANDA ANDA200651 REMEDYREPACK INC. GABAPENTIN 800 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2323-1)
70518-2323-3 70518-2323 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET, FILM COATED ORAL 20201223 N/A ANDA ANDA200651 REMEDYREPACK INC. GABAPENTIN 800 mg/1 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2323-3)
70518-2323-4 70518-2323 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET, FILM COATED ORAL 20260324 N/A ANDA ANDA200651 REMEDYREPACK INC. GABAPENTIN 800 mg/1 100 POUCH in 1 BOX (70518-2323-4) / 1 TABLET, FILM COATED in 1 POUCH (70518-2323-5)
70518-2356-0 70518-2356 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET, FILM COATED ORAL 20191009 N/A ANDA ANDA200651 REMEDYREPACK INC. GABAPENTIN 600 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2356-0)
70518-2356-1 70518-2356 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET, FILM COATED ORAL 20191021 N/A ANDA ANDA200651 REMEDYREPACK INC. GABAPENTIN 600 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2356-1)
55154-3357-0 55154-3357 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET, FILM COATED ORAL 20111006 N/A ANDA ANDA200651 Cardinal Health 107, LLC GABAPENTIN 600 mg/1 10 BLISTER PACK in 1 BAG (55154-3357-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
55154-3366-0 55154-3366 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET, FILM COATED ORAL 20111006 N/A ANDA ANDA200651 Cardinal Health 107, LLC GABAPENTIN 800 mg/1 10 BLISTER PACK in 1 BAG (55154-3366-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
70518-2616-6 70518-2616 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET, FILM COATED ORAL 20250618 N/A ANDA ANDA200651 REMEDYREPACK INC. GABAPENTIN 600 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2616-6)
65862-523-01 65862-523 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET, FILM COATED ORAL 20111006 N/A ANDA ANDA200651 Aurobindo Pharma Limited GABAPENTIN 600 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65862-523-01)
65862-523-05 65862-523 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET, FILM COATED ORAL 20111006 N/A ANDA ANDA200651 Aurobindo Pharma Limited GABAPENTIN 600 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65862-523-05)
65862-523-26 65862-523 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET, FILM COATED ORAL 20111006 N/A ANDA ANDA200651 Aurobindo Pharma Limited GABAPENTIN 600 mg/1 2500 TABLET, FILM COATED in 1 BOTTLE (65862-523-26)
65862-523-90 65862-523 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET, FILM COATED ORAL 20111006 N/A ANDA ANDA200651 Aurobindo Pharma Limited GABAPENTIN 600 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (65862-523-90)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase