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
68788-8343-3 68788-8343 HUMAN PRESCRIPTION DRUG GLYBURIDE GLYBURIDE TABLET ORAL 20230203 N/A ANDA ANDA090937 Preferred Pharmaceuticals Inc. GLYBURIDE 5 mg/1 30 TABLET in 1 BOTTLE (68788-8343-3)
63187-667-30 63187-667 HUMAN PRESCRIPTION DRUG Glyburide Glyburide TABLET ORAL 20181201 N/A ANDA ANDA090937 Proficient Rx LP GLYBURIDE 5 mg/1 30 TABLET in 1 BOTTLE (63187-667-30)
63187-667-60 63187-667 HUMAN PRESCRIPTION DRUG Glyburide Glyburide TABLET ORAL 20181201 N/A ANDA ANDA090937 Proficient Rx LP GLYBURIDE 5 mg/1 60 TABLET in 1 BOTTLE (63187-667-60)
63187-667-90 63187-667 HUMAN PRESCRIPTION DRUG Glyburide Glyburide TABLET ORAL 20181201 N/A ANDA ANDA090937 Proficient Rx LP GLYBURIDE 5 mg/1 90 TABLET in 1 BOTTLE (63187-667-90)
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)
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)
23155-058-01 23155-058 HUMAN PRESCRIPTION DRUG GLYBURIDE GLYBURIDE TABLET ORAL 20101005 N/A ANDA ANDA090937 Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. GLYBURIDE 5 mg/1 100 TABLET in 1 BOTTLE (23155-058-01)
23155-058-10 23155-058 HUMAN PRESCRIPTION DRUG GLYBURIDE GLYBURIDE TABLET ORAL 20101005 N/A ANDA ANDA090937 Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. GLYBURIDE 5 mg/1 1000 TABLET in 1 BOTTLE (23155-058-10)
68071-5217-0 68071-5217 HUMAN PRESCRIPTION DRUG GLYBURIDE GLYBURIDE TABLET ORAL 20200318 N/A ANDA ANDA090937 NuCare Pharmaceuticals,Inc. GLYBURIDE 2.5 mg/1 100 TABLET in 1 BOTTLE (68071-5217-0)
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)
68788-8343-6 68788-8343 HUMAN PRESCRIPTION DRUG GLYBURIDE GLYBURIDE TABLET ORAL 20230203 N/A ANDA ANDA090937 Preferred Pharmaceuticals Inc. GLYBURIDE 5 mg/1 60 TABLET in 1 BOTTLE (68788-8343-6)
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)
68788-8343-9 68788-8343 HUMAN PRESCRIPTION DRUG GLYBURIDE GLYBURIDE TABLET ORAL 20230203 N/A ANDA ANDA090937 Preferred Pharmaceuticals Inc. GLYBURIDE 5 mg/1 90 TABLET in 1 BOTTLE (68788-8343-9)
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