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=ANDA203379"
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
71335-2771-5 71335-2771 HUMAN PRESCRIPTION DRUG Glyburide Glyburide TABLET ORAL 20251003 N/A ANDA ANDA203379 Bryant Ranch Prepack GLYBURIDE 5 mg/1 90 TABLET in 1 BOTTLE (71335-2771-5)
71335-2771-6 71335-2771 HUMAN PRESCRIPTION DRUG Glyburide Glyburide TABLET ORAL 20251003 N/A ANDA ANDA203379 Bryant Ranch Prepack GLYBURIDE 5 mg/1 180 TABLET in 1 BOTTLE (71335-2771-6)
75834-204-00 75834-204 HUMAN PRESCRIPTION DRUG GLYBURIDE GLYBURIDE TABLET ORAL 20190125 N/A ANDA ANDA203379 Nivagen Pharmaceuticals, Inc. GLYBURIDE 5 mg/1 1000 TABLET in 1 BOTTLE (75834-204-00)
75834-204-01 75834-204 HUMAN PRESCRIPTION DRUG GLYBURIDE GLYBURIDE TABLET ORAL 20190125 N/A ANDA ANDA203379 Nivagen Pharmaceuticals, Inc. GLYBURIDE 5 mg/1 100 TABLET in 1 BOTTLE (75834-204-01)
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