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=ANDA216282"
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
71335-3054-7 71335-3054 HUMAN PRESCRIPTION DRUG Dexamethasone Dexamethasone TABLET ORAL 20260205 N/A ANDA ANDA216282 Bryant Ranch Prepack DEXAMETHASONE 4 mg/1 28 TABLET in 1 BOTTLE (71335-3054-7)
71335-3054-8 71335-3054 HUMAN PRESCRIPTION DRUG Dexamethasone Dexamethasone TABLET ORAL 20260205 N/A ANDA ANDA216282 Bryant Ranch Prepack DEXAMETHASONE 4 mg/1 90 TABLET in 1 BOTTLE (71335-3054-8)
71335-3054-9 71335-3054 HUMAN PRESCRIPTION DRUG Dexamethasone Dexamethasone TABLET ORAL 20260205 N/A ANDA ANDA216282 Bryant Ranch Prepack DEXAMETHASONE 4 mg/1 10 TABLET in 1 BOTTLE (71335-3054-9)
68788-8763-0 68788-8763 HUMAN PRESCRIPTION DRUG Dexamethasone Dexamethasone TABLET ORAL 20241111 N/A ANDA ANDA216282 Preferred Pharmaceuticals Inc. DEXAMETHASONE .75 mg/1 100 TABLET in 1 BOTTLE (68788-8763-0)
68788-8763-1 68788-8763 HUMAN PRESCRIPTION DRUG Dexamethasone Dexamethasone TABLET ORAL 20241111 N/A ANDA ANDA216282 Preferred Pharmaceuticals Inc. DEXAMETHASONE .75 mg/1 12 TABLET in 1 BOTTLE (68788-8763-1)
68788-8763-2 68788-8763 HUMAN PRESCRIPTION DRUG Dexamethasone Dexamethasone TABLET ORAL 20241111 N/A ANDA ANDA216282 Preferred Pharmaceuticals Inc. DEXAMETHASONE .75 mg/1 21 TABLET in 1 BOTTLE (68788-8763-2)
68788-8763-3 68788-8763 HUMAN PRESCRIPTION DRUG Dexamethasone Dexamethasone TABLET ORAL 20241111 N/A ANDA ANDA216282 Preferred Pharmaceuticals Inc. DEXAMETHASONE .75 mg/1 30 TABLET in 1 BOTTLE (68788-8763-3)
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