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=ANDA078181"
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
68001-177-00 68001-177 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20140226 20250831 ANDA ANDA078181 BluePoint Laboratories GLIMEPIRIDE 1 mg/1 100 TABLET in 1 BOTTLE (68001-177-00)
68001-177-03 68001-177 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20140226 20250831 ANDA ANDA078181 BluePoint Laboratories GLIMEPIRIDE 1 mg/1 500 TABLET in 1 BOTTLE (68001-177-03)
60760-248-90 60760-248 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20171226 N/A ANDA ANDA078181 St. Mary’s Medical Park Pharmacy GLIMEPIRIDE 4 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (60760-248-90)
61919-250-04 61919-250 HUMAN PRESCRIPTION DRUG GLIMEPIRIDE GLIMEPIRIDE TABLET ORAL 20160204 N/A ANDA ANDA078181 DIRECT RX GLIMEPIRIDE 4 mg/1 4 TABLET in 1 BOTTLE (61919-250-04)
61919-250-30 61919-250 HUMAN PRESCRIPTION DRUG GLIMEPIRIDE GLIMEPIRIDE TABLET ORAL 20160204 N/A ANDA ANDA078181 DIRECT RX GLIMEPIRIDE 4 mg/1 30 TABLET in 1 BOTTLE (61919-250-30)
61919-250-60 61919-250 HUMAN PRESCRIPTION DRUG GLIMEPIRIDE GLIMEPIRIDE TABLET ORAL 20160204 N/A ANDA ANDA078181 DIRECT RX GLIMEPIRIDE 4 mg/1 60 TABLET in 1 BOTTLE (61919-250-60)
61919-250-82 61919-250 HUMAN PRESCRIPTION DRUG GLIMEPIRIDE GLIMEPIRIDE TABLET ORAL 20160204 N/A ANDA ANDA078181 DIRECT RX GLIMEPIRIDE 4 mg/1 180 TABLET in 1 BOTTLE (61919-250-82)
61919-250-90 61919-250 HUMAN PRESCRIPTION DRUG GLIMEPIRIDE GLIMEPIRIDE TABLET ORAL 20160204 N/A ANDA ANDA078181 DIRECT RX GLIMEPIRIDE 4 mg/1 90 TABLET in 1 BOTTLE (61919-250-90)
16729-002-01 16729-002 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20070823 N/A ANDA ANDA078181 Accord Healthcare Inc GLIMEPIRIDE 2 mg/1 100 TABLET in 1 BOTTLE (16729-002-01)
16729-002-16 16729-002 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20160824 N/A ANDA ANDA078181 Accord Healthcare Inc GLIMEPIRIDE 2 mg/1 500 TABLET in 1 BOTTLE (16729-002-16)
63187-641-30 63187-641 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20181201 N/A ANDA ANDA078181 Proficient Rx LP GLIMEPIRIDE 2 mg/1 30 TABLET in 1 BOTTLE (63187-641-30)
63187-641-60 63187-641 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20181201 N/A ANDA ANDA078181 Proficient Rx LP GLIMEPIRIDE 2 mg/1 60 TABLET in 1 BOTTLE (63187-641-60)
68001-179-00 68001-179 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20140226 20250831 ANDA ANDA078181 BluePoint Laboratories GLIMEPIRIDE 4 mg/1 100 TABLET in 1 BOTTLE (68001-179-00)
68001-179-03 68001-179 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20140226 20250831 ANDA ANDA078181 BluePoint Laboratories GLIMEPIRIDE 4 mg/1 500 TABLET in 1 BOTTLE (68001-179-03)
51655-383-26 51655-383 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20230120 N/A ANDA ANDA078181 Northwind Pharmaceuticals, LLC GLIMEPIRIDE 2 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (51655-383-26)
51655-383-52 51655-383 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20220907 N/A ANDA ANDA078181 Northwind Pharmaceuticals, LLC GLIMEPIRIDE 2 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (51655-383-52)
68788-8095-1 68788-8095 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20211006 N/A ANDA ANDA078181 Preferred Pharmaceuticals Inc. GLIMEPIRIDE 2 mg/1 100 TABLET in 1 BOTTLE (68788-8095-1)
68788-8095-3 68788-8095 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20211006 N/A ANDA ANDA078181 Preferred Pharmaceuticals Inc. GLIMEPIRIDE 2 mg/1 30 TABLET in 1 BOTTLE (68788-8095-3)
68788-8095-6 68788-8095 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20211006 N/A ANDA ANDA078181 Preferred Pharmaceuticals Inc. GLIMEPIRIDE 2 mg/1 60 TABLET in 1 BOTTLE (68788-8095-6)
68788-8095-9 68788-8095 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20211006 N/A ANDA ANDA078181 Preferred Pharmaceuticals Inc. GLIMEPIRIDE 2 mg/1 90 TABLET in 1 BOTTLE (68788-8095-9)
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