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=ANDA202764"
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
76282-405-01 76282-405 HUMAN PRESCRIPTION DRUG GABAPENTIN gabapentin TABLET, FILM COATED ORAL 20121102 N/A ANDA ANDA202764 Exelan Pharmaceuticals Inc. GABAPENTIN 600 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (76282-405-01)
76282-405-05 76282-405 HUMAN PRESCRIPTION DRUG GABAPENTIN gabapentin TABLET, FILM COATED ORAL 20121102 N/A ANDA ANDA202764 Exelan Pharmaceuticals Inc. GABAPENTIN 600 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (76282-405-05)
76282-405-30 76282-405 HUMAN PRESCRIPTION DRUG GABAPENTIN gabapentin TABLET, FILM COATED ORAL 20121102 N/A ANDA ANDA202764 Exelan Pharmaceuticals Inc. GABAPENTIN 600 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76282-405-30)
76282-405-90 76282-405 HUMAN PRESCRIPTION DRUG GABAPENTIN gabapentin TABLET, FILM COATED ORAL 20121102 N/A ANDA ANDA202764 Exelan Pharmaceuticals Inc. GABAPENTIN 600 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (76282-405-90)
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)
76282-406-01 76282-406 HUMAN PRESCRIPTION DRUG GABAPENTIN gabapentin TABLET, FILM COATED ORAL 20121102 N/A ANDA ANDA202764 Exelan Pharmaceuticals Inc. GABAPENTIN 800 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (76282-406-01)
76282-406-05 76282-406 HUMAN PRESCRIPTION DRUG GABAPENTIN gabapentin TABLET, FILM COATED ORAL 20121102 N/A ANDA ANDA202764 Exelan Pharmaceuticals Inc. GABAPENTIN 800 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (76282-406-05)
76282-406-30 76282-406 HUMAN PRESCRIPTION DRUG GABAPENTIN gabapentin TABLET, FILM COATED ORAL 20121102 N/A ANDA ANDA202764 Exelan Pharmaceuticals Inc. GABAPENTIN 800 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76282-406-30)
76282-406-90 76282-406 HUMAN PRESCRIPTION DRUG GABAPENTIN gabapentin TABLET, FILM COATED ORAL 20121102 N/A ANDA ANDA202764 Exelan Pharmaceuticals Inc. GABAPENTIN 800 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (76282-406-90)
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)
63187-785-30 63187-785 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20161201 N/A ANDA ANDA202764 Proficient Rx LP GABAPENTIN 600 mg/1 30 TABLET in 1 BOTTLE (63187-785-30)
63187-785-60 63187-785 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20161201 N/A ANDA ANDA202764 Proficient Rx LP GABAPENTIN 600 mg/1 60 TABLET in 1 BOTTLE (63187-785-60)
63187-785-72 63187-785 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20161201 N/A ANDA ANDA202764 Proficient Rx LP GABAPENTIN 600 mg/1 120 TABLET in 1 BOTTLE (63187-785-72)
63187-785-90 63187-785 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET ORAL 20161201 N/A ANDA ANDA202764 Proficient Rx LP GABAPENTIN 600 mg/1 90 TABLET in 1 BOTTLE (63187-785-90)
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