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=ANDA207057"
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
50090-4445-2 50090-4445 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET, COATED ORAL 20190801 N/A ANDA ANDA207057 A-S Medication Solutions GABAPENTIN 600 mg/1 30 TABLET, COATED in 1 BOTTLE (50090-4445-2)
83301-0001-1 83301-0001 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET, COATED ORAL 20240101 N/A ANDA ANDA207057 Mullan Pharmaceutical Inc. GABAPENTIN 600 mg/1 100 TABLET, COATED in 1 BOTTLE, PLASTIC (83301-0001-1)
83301-0001-2 83301-0001 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET, COATED ORAL 20240101 N/A ANDA ANDA207057 Mullan Pharmaceutical Inc. GABAPENTIN 600 mg/1 500 TABLET, COATED in 1 BOTTLE, PLASTIC (83301-0001-2)
83301-0002-1 83301-0002 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET, COATED ORAL 20240101 N/A ANDA ANDA207057 Mullan Pharmaceutical Inc. GABAPENTIN 800 mg/1 100 TABLET, COATED in 1 BOTTLE, PLASTIC (83301-0002-1)
83301-0002-2 83301-0002 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET, COATED ORAL 20240101 N/A ANDA ANDA207057 Mullan Pharmaceutical Inc. GABAPENTIN 800 mg/1 500 TABLET, COATED in 1 BOTTLE, PLASTIC (83301-0002-2)
69367-346-05 69367-346 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET, COATED ORAL 20211101 N/A ANDA ANDA207057 Westminster Pharmaceuticals, LLC GABAPENTIN 600 mg/1 500 TABLET, COATED in 1 BOTTLE, PLASTIC (69367-346-05)
69367-347-05 69367-347 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET, COATED ORAL 20211101 N/A ANDA ANDA207057 Westminster Pharmaceuticals, LLC GABAPENTIN 800 mg/1 500 TABLET, COATED in 1 BOTTLE, PLASTIC (69367-347-05)
68094-489-50 68094-489 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET, COATED ORAL 20240215 N/A ANDA ANDA207057 Precision Dose, Inc. GABAPENTIN 800 mg/1 100 TABLET, COATED in 1 BOTTLE (68094-489-50)
68094-489-60 68094-489 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET, COATED ORAL 20240215 N/A ANDA ANDA207057 Precision Dose, Inc. GABAPENTIN 800 mg/1 500 TABLET, COATED in 1 BOTTLE (68094-489-60)
68094-589-50 68094-589 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET, COATED ORAL 20240215 N/A ANDA ANDA207057 Precision Dose, Inc. GABAPENTIN 600 mg/1 100 TABLET, COATED in 1 BOTTLE (68094-589-50)
68094-589-60 68094-589 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET, COATED ORAL 20240215 N/A ANDA ANDA207057 Precision Dose, Inc. GABAPENTIN 600 mg/1 500 TABLET, COATED in 1 BOTTLE (68094-589-60)
80425-0201-1 80425-0201 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET, COATED ORAL 20221028 N/A ANDA ANDA207057 Advanced Rx Pharmacy of Tennessee, LLC GABAPENTIN 600 mg/1 30 TABLET, COATED in 1 BOTTLE (80425-0201-1)
80425-0201-2 80425-0201 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET, COATED ORAL 20221028 N/A ANDA ANDA207057 Advanced Rx Pharmacy of Tennessee, LLC GABAPENTIN 600 mg/1 60 TABLET, COATED in 1 BOTTLE (80425-0201-2)
80425-0201-3 80425-0201 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET, COATED ORAL 20221028 N/A ANDA ANDA207057 Advanced Rx Pharmacy of Tennessee, LLC GABAPENTIN 600 mg/1 90 TABLET, COATED in 1 BOTTLE (80425-0201-3)
80425-0201-4 80425-0201 HUMAN PRESCRIPTION DRUG Gabapentin Gabapentin TABLET, COATED ORAL 20221028 N/A ANDA ANDA207057 Advanced Rx Pharmacy of Tennessee, LLC GABAPENTIN 600 mg/1 120 TABLET, COATED in 1 BOTTLE (80425-0201-4)
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