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=ANDA074388"
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
53002-4171-0 53002-4171 HUMAN PRESCRIPTION DRUG Glyburide Glyburide TABLET ORAL 20240101 N/A ANDA ANDA074388 RPK Pharmaceuticals, Inc. GLYBURIDE 5 mg/1 100 TABLET in 1 BOTTLE (53002-4171-0)
53002-4171-3 53002-4171 HUMAN PRESCRIPTION DRUG Glyburide Glyburide TABLET ORAL 20240101 N/A ANDA ANDA074388 RPK Pharmaceuticals, Inc. GLYBURIDE 5 mg/1 30 TABLET in 1 BOTTLE (53002-4171-3)
63187-848-30 63187-848 HUMAN PRESCRIPTION DRUG Glyburide Glyburide TABLET ORAL 19950830 N/A ANDA ANDA074388 Proficient Rx LP GLYBURIDE 2.5 mg/1 30 TABLET in 1 BOTTLE (63187-848-30)
63187-848-60 63187-848 HUMAN PRESCRIPTION DRUG Glyburide Glyburide TABLET ORAL 19950830 N/A ANDA ANDA074388 Proficient Rx LP GLYBURIDE 2.5 mg/1 60 TABLET in 1 BOTTLE (63187-848-60)
63187-848-90 63187-848 HUMAN PRESCRIPTION DRUG Glyburide Glyburide TABLET ORAL 20100330 N/A ANDA ANDA074388 Proficient Rx LP GLYBURIDE 2.5 mg/1 90 TABLET in 1 BOTTLE (63187-848-90)
50090-6607-0 50090-6607 HUMAN PRESCRIPTION DRUG Glyburide Glyburide TABLET ORAL 20230822 N/A ANDA ANDA074388 A-S Medication Solutions GLYBURIDE 5 mg/1 90 TABLET in 1 BOTTLE (50090-6607-0)
68071-2189-3 68071-2189 HUMAN PRESCRIPTION DRUG Glyburide Glyburide TABLET ORAL 20170323 N/A ANDA ANDA074388 NuCare Pharmaceuticals, Inc. GLYBURIDE 2.5 mg/1 30 TABLET in 1 BOTTLE (68071-2189-3)
68071-2189-6 68071-2189 HUMAN PRESCRIPTION DRUG Glyburide Glyburide TABLET ORAL 20170323 N/A ANDA ANDA074388 NuCare Pharmaceuticals, Inc. GLYBURIDE 2.5 mg/1 60 TABLET in 1 BOTTLE (68071-2189-6)
68071-2189-8 68071-2189 HUMAN PRESCRIPTION DRUG Glyburide Glyburide TABLET ORAL 20230620 N/A ANDA ANDA074388 NuCare Pharmaceuticals, Inc. GLYBURIDE 2.5 mg/1 180 TABLET in 1 BOTTLE (68071-2189-8)
68071-2189-9 68071-2189 HUMAN PRESCRIPTION DRUG Glyburide Glyburide TABLET ORAL 20170323 N/A ANDA ANDA074388 NuCare Pharmaceuticals, Inc. GLYBURIDE 2.5 mg/1 90 TABLET in 1 BOTTLE (68071-2189-9)
0093-8342-01 0093-8342 HUMAN PRESCRIPTION DRUG Glyburide Glyburide TABLET ORAL 19950830 N/A ANDA ANDA074388 Teva Pharmaceuticals USA, Inc. GLYBURIDE 1.25 mg/1 100 TABLET in 1 BOTTLE (0093-8342-01)
0093-8343-01 0093-8343 HUMAN PRESCRIPTION DRUG Glyburide Glyburide TABLET ORAL 19950830 N/A ANDA ANDA074388 Teva Pharmaceuticals USA, Inc. GLYBURIDE 2.5 mg/1 100 TABLET in 1 BOTTLE (0093-8343-01)
0093-8343-05 0093-8343 HUMAN PRESCRIPTION DRUG Glyburide Glyburide TABLET ORAL 19950830 N/A ANDA ANDA074388 Teva Pharmaceuticals USA, Inc. GLYBURIDE 2.5 mg/1 500 TABLET in 1 BOTTLE (0093-8343-05)
0093-8343-10 0093-8343 HUMAN PRESCRIPTION DRUG Glyburide Glyburide TABLET ORAL 19950830 N/A ANDA ANDA074388 Teva Pharmaceuticals USA, Inc. GLYBURIDE 2.5 mg/1 1000 TABLET in 1 BOTTLE (0093-8343-10)
0093-8343-98 0093-8343 HUMAN PRESCRIPTION DRUG Glyburide Glyburide TABLET ORAL 20100330 N/A ANDA ANDA074388 Teva Pharmaceuticals USA, Inc. GLYBURIDE 2.5 mg/1 90 TABLET in 1 BOTTLE (0093-8343-98)
0093-8344-01 0093-8344 HUMAN PRESCRIPTION DRUG Glyburide Glyburide TABLET ORAL 19950830 N/A ANDA ANDA074388 Teva Pharmaceuticals USA, Inc. GLYBURIDE 5 mg/1 100 TABLET in 1 BOTTLE (0093-8344-01)
0093-8344-05 0093-8344 HUMAN PRESCRIPTION DRUG Glyburide Glyburide TABLET ORAL 19950830 N/A ANDA ANDA074388 Teva Pharmaceuticals USA, Inc. GLYBURIDE 5 mg/1 500 TABLET in 1 BOTTLE (0093-8344-05)
0093-8344-10 0093-8344 HUMAN PRESCRIPTION DRUG Glyburide Glyburide TABLET ORAL 19950830 N/A ANDA ANDA074388 Teva Pharmaceuticals USA, Inc. GLYBURIDE 5 mg/1 1000 TABLET in 1 BOTTLE (0093-8344-10)
0093-8344-98 0093-8344 HUMAN PRESCRIPTION DRUG Glyburide Glyburide TABLET ORAL 20100330 N/A ANDA ANDA074388 Teva Pharmaceuticals USA, Inc. GLYBURIDE 5 mg/1 90 TABLET in 1 BOTTLE (0093-8344-98)
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