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
53002-4170-3 53002-4170 HUMAN PRESCRIPTION DRUG GLYBURIDE GLYBURIDE TABLET ORAL 20200101 N/A ANDA ANDA090937 RPK Pharmaceuticals, Inc. GLYBURIDE 5 mg/1 30 TABLET in 1 BOTTLE (53002-4170-3)
53002-4170-6 53002-4170 HUMAN PRESCRIPTION DRUG GLYBURIDE GLYBURIDE TABLET ORAL 20200101 N/A ANDA ANDA090937 RPK Pharmaceuticals, Inc. GLYBURIDE 5 mg/1 60 TABLET in 1 BOTTLE (53002-4170-6)
53002-4170-0 53002-4170 HUMAN PRESCRIPTION DRUG GLYBURIDE GLYBURIDE TABLET ORAL 20200101 N/A ANDA ANDA090937 RPK Pharmaceuticals, Inc. GLYBURIDE 5 mg/1 100 TABLET in 1 BOTTLE (53002-4170-0)
50090-0495-0 50090-0495 HUMAN PRESCRIPTION DRUG GLYBURIDE GLYBURIDE TABLET ORAL 20160629 N/A ANDA ANDA090937 A-S Medication Solutions GLYBURIDE 5 mg/1 30 TABLET in 1 BOTTLE (50090-0495-0)
50090-0495-1 50090-0495 HUMAN PRESCRIPTION DRUG GLYBURIDE GLYBURIDE TABLET ORAL 20160629 N/A ANDA ANDA090937 A-S Medication Solutions GLYBURIDE 5 mg/1 100 TABLET in 1 BOTTLE (50090-0495-1)
50090-0495-2 50090-0495 HUMAN PRESCRIPTION DRUG GLYBURIDE GLYBURIDE TABLET ORAL 20160629 N/A ANDA ANDA090937 A-S Medication Solutions GLYBURIDE 5 mg/1 60 TABLET in 1 BOTTLE (50090-0495-2)
50090-0495-8 50090-0495 HUMAN PRESCRIPTION DRUG GLYBURIDE GLYBURIDE TABLET ORAL 20160629 N/A ANDA ANDA090937 A-S Medication Solutions GLYBURIDE 5 mg/1 200 TABLET in 1 BOTTLE (50090-0495-8)
50090-0495-9 50090-0495 HUMAN PRESCRIPTION DRUG GLYBURIDE GLYBURIDE TABLET ORAL 20160629 N/A ANDA ANDA090937 A-S Medication Solutions GLYBURIDE 5 mg/1 90 TABLET in 1 BOTTLE (50090-0495-9)
68788-8343-1 68788-8343 HUMAN PRESCRIPTION DRUG GLYBURIDE GLYBURIDE TABLET ORAL 20230203 N/A ANDA ANDA090937 Preferred Pharmaceuticals Inc. GLYBURIDE 5 mg/1 100 TABLET in 1 BOTTLE (68788-8343-1)
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)
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)
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)
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)
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)
51655-659-52 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)
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