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=ANDA090937"
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
71335-0069-1 71335-0069 HUMAN PRESCRIPTION DRUG GLYBURIDE GLYBURIDE TABLET ORAL 20181108 N/A ANDA ANDA090937 Bryant Ranch Prepack GLYBURIDE 2.5 mg/1 30 TABLET in 1 BOTTLE (71335-0069-1)
71335-0069-2 71335-0069 HUMAN PRESCRIPTION DRUG GLYBURIDE GLYBURIDE TABLET ORAL 20211227 N/A ANDA ANDA090937 Bryant Ranch Prepack GLYBURIDE 2.5 mg/1 60 TABLET in 1 BOTTLE (71335-0069-2)
71335-0069-3 71335-0069 HUMAN PRESCRIPTION DRUG GLYBURIDE GLYBURIDE TABLET ORAL 20191120 N/A ANDA ANDA090937 Bryant Ranch Prepack GLYBURIDE 2.5 mg/1 90 TABLET in 1 BOTTLE (71335-0069-3)
62135-583-30 62135-583 HUMAN PRESCRIPTION DRUG GLYBURIDE GLYBURIDE TABLET ORAL 20230509 N/A ANDA ANDA090937 Chartwell RX, LLC GLYBURIDE 1.25 mg/1 30 TABLET in 1 BOTTLE (62135-583-30)
62135-584-30 62135-584 HUMAN PRESCRIPTION DRUG GLYBURIDE GLYBURIDE TABLET ORAL 20230509 N/A ANDA ANDA090937 Chartwell RX, LLC GLYBURIDE 2.5 mg/1 30 TABLET in 1 BOTTLE (62135-584-30)
62135-585-90 62135-585 HUMAN PRESCRIPTION DRUG GLYBURIDE GLYBURIDE TABLET ORAL 20230509 N/A ANDA ANDA090937 Chartwell RX, LLC GLYBURIDE 5 mg/1 90 TABLET in 1 BOTTLE (62135-585-90)
71335-0150-1 71335-0150 HUMAN PRESCRIPTION DRUG GLYBURIDE GLYBURIDE TABLET ORAL 20220209 N/A ANDA ANDA090937 Bryant Ranch Prepack GLYBURIDE 5 mg/1 30 TABLET in 1 BOTTLE (71335-0150-1)
71335-0150-2 71335-0150 HUMAN PRESCRIPTION DRUG GLYBURIDE GLYBURIDE TABLET ORAL 20220209 N/A ANDA ANDA090937 Bryant Ranch Prepack GLYBURIDE 5 mg/1 120 TABLET in 1 BOTTLE (71335-0150-2)
71335-0150-3 71335-0150 HUMAN PRESCRIPTION DRUG GLYBURIDE GLYBURIDE TABLET ORAL 20220209 N/A ANDA ANDA090937 Bryant Ranch Prepack GLYBURIDE 5 mg/1 100 TABLET in 1 BOTTLE (71335-0150-3)
71335-0150-4 71335-0150 HUMAN PRESCRIPTION DRUG GLYBURIDE GLYBURIDE TABLET ORAL 20220209 N/A ANDA ANDA090937 Bryant Ranch Prepack GLYBURIDE 5 mg/1 60 TABLET in 1 BOTTLE (71335-0150-4)
71335-0150-5 71335-0150 HUMAN PRESCRIPTION DRUG GLYBURIDE GLYBURIDE TABLET ORAL 20220209 N/A ANDA ANDA090937 Bryant Ranch Prepack GLYBURIDE 5 mg/1 90 TABLET in 1 BOTTLE (71335-0150-5)
71335-0150-6 71335-0150 HUMAN PRESCRIPTION DRUG GLYBURIDE GLYBURIDE TABLET ORAL 20220209 N/A ANDA ANDA090937 Bryant Ranch Prepack GLYBURIDE 5 mg/1 180 TABLET in 1 BOTTLE (71335-0150-6)
51655-492-25 51655-492 HUMAN PRESCRIPTION DRUG GLYBURIDE GLYBURIDE TABLET ORAL 20220209 N/A ANDA ANDA090937 Northwind Pharmaceuticals, LLC GLYBURIDE 5 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (51655-492-25)
51655-492-26 51655-492 HUMAN PRESCRIPTION DRUG GLYBURIDE GLYBURIDE TABLET ORAL 20231116 N/A ANDA ANDA090937 Northwind Pharmaceuticals, LLC GLYBURIDE 5 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (51655-492-26)
51655-492-52 51655-492 HUMAN PRESCRIPTION DRUG GLYBURIDE GLYBURIDE TABLET ORAL 20210107 N/A ANDA ANDA090937 Northwind Pharmaceuticals, LLC GLYBURIDE 5 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (51655-492-52)
51655-659-52 51655-659 HUMAN PRESCRIPTION DRUG GLYBURIDE GLYBURIDE TABLET ORAL 20210323 N/A ANDA ANDA090937 Northwind Pharmaceuticals GLYBURIDE 2.5 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (51655-659-52)
50090-5776-0 50090-5776 HUMAN PRESCRIPTION DRUG GLYBURIDE GLYBURIDE TABLET ORAL 20211007 N/A ANDA ANDA090937 A-S Medication Solutions GLYBURIDE 2.5 mg/1 30 TABLET in 1 BOTTLE (50090-5776-0)
50090-5776-2 50090-5776 HUMAN PRESCRIPTION DRUG GLYBURIDE GLYBURIDE TABLET ORAL 20211007 N/A ANDA ANDA090937 A-S Medication Solutions GLYBURIDE 2.5 mg/1 200 TABLET in 1 BOTTLE (50090-5776-2)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase