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=ANDA207442"
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
80425-0261-1 80425-0261 HUMAN PRESCRIPTION DRUG Dexamethasone Sodium Phosphate Dexamethasone Sodium Phosphate INJECTION INTRAMUSCULAR; INTRAVENOUS 20230216 N/A ANDA ANDA207442 Advanced Rx Pharmacy of Tennessee, LLC DEXAMETHASONE SODIUM PHOSPHATE 10 mg/mL 25 VIAL in 1 CARTON (80425-0261-1) / 1 mL in 1 VIAL
70069-021-25 70069-021 HUMAN PRESCRIPTION DRUG Dexamethasone Sodium Phosphate Dexamethasone Sodium Phosphate INJECTION INTRAMUSCULAR; INTRAVENOUS 20180419 N/A ANDA ANDA207442 Somerset Therapeutics, LLC DEXAMETHASONE SODIUM PHOSPHATE 10 mg/mL 25 VIAL in 1 CARTON (70069-021-25) / 1 mL in 1 VIAL (70069-021-01)
70518-1922-1 70518-1922 HUMAN PRESCRIPTION DRUG Dexamethasone Sodium Phosphate Dexamethasone Sodium Phosphate INJECTION INTRAMUSCULAR; INTRAVENOUS 20190228 N/A ANDA ANDA207442 REMEDYREPACK INC. DEXAMETHASONE SODIUM PHOSPHATE 10 mg/mL 25 VIAL in 1 CARTON (70518-1922-1) / 1 mL in 1 VIAL (70518-1922-0)
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