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=ANDA217066"
符合检索条件的记录共 4 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
70710-1835-1 70710-1835 HUMAN PRESCRIPTION DRUG LEVOTHYROXINE SODIUM levothyroxine sodium INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAVENOUS 20241101 N/A ANDA ANDA217066 Zydus Pharmaceuticals USA Inc. LEVOTHYROXINE SODIUM ANHYDROUS 500 ug/5mL 1 VIAL, SINGLE-DOSE in 1 CARTON (70710-1835-1) / 5 mL in 1 VIAL, SINGLE-DOSE
70710-1833-1 70710-1833 HUMAN PRESCRIPTION DRUG LEVOTHYROXINE SODIUM levothyroxine sodium INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAVENOUS 20241101 N/A ANDA ANDA217066 Zydus Pharmaceuticals USA Inc. LEVOTHYROXINE SODIUM ANHYDROUS 100 ug/5mL 1 VIAL, SINGLE-DOSE in 1 CARTON (70710-1833-1) / 5 mL in 1 VIAL, SINGLE-DOSE
70710-1834-1 70710-1834 HUMAN PRESCRIPTION DRUG LEVOTHYROXINE SODIUM levothyroxine sodium INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAVENOUS 20241101 N/A ANDA ANDA217066 Zydus Pharmaceuticals USA Inc. LEVOTHYROXINE SODIUM ANHYDROUS 200 ug/5mL 1 VIAL, SINGLE-DOSE in 1 CARTON (70710-1834-1) / 5 mL in 1 VIAL, SINGLE-DOSE
70771-1818-1 70771-1818 HUMAN PRESCRIPTION DRUG LEVOTHYROXINE SODIUM levothyroxine sodium INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAVENOUS 20241101 N/A ANDA ANDA217066 Zydus Lifesciences Limited LEVOTHYROXINE SODIUM ANHYDROUS 100 ug/5mL 1 VIAL, SINGLE-DOSE in 1 CARTON (70771-1818-1) / 5 mL in 1 VIAL, SINGLE-DOSE
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