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=ANDA214870"
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
0781-3522-75 0781-3522 HUMAN PRESCRIPTION DRUG METHYLPREDNISOLONE ACETATE METHYLPREDNISOLONE ACETATE INJECTION, SUSPENSION INTRALESIONAL; INTRAMUSCULAR; INTRASYNOVIAL; SOFT TISSUE 20240314 N/A ANDA ANDA214870 Sandoz Inc. METHYLPREDNISOLONE ACETATE 40 mg/mL 1 VIAL, MULTI-DOSE in 1 CARTON (0781-3522-75) / 5 mL in 1 VIAL, MULTI-DOSE
0781-3522-70 0781-3522 HUMAN PRESCRIPTION DRUG METHYLPREDNISOLONE ACETATE METHYLPREDNISOLONE ACETATE INJECTION, SUSPENSION INTRALESIONAL; INTRAMUSCULAR; INTRASYNOVIAL; SOFT TISSUE 20240314 N/A ANDA ANDA214870 Sandoz Inc. METHYLPREDNISOLONE ACETATE 40 mg/mL 1 VIAL, MULTI-DOSE in 1 CARTON (0781-3522-70) / 10 mL in 1 VIAL, MULTI-DOSE
0781-3516-75 0781-3516 HUMAN PRESCRIPTION DRUG METHYLPREDNISOLONE ACETATE METHYLPREDNISOLONE ACETATE INJECTION, SUSPENSION INTRALESIONAL; INTRAMUSCULAR; INTRASYNOVIAL; SOFT TISSUE 20230208 N/A ANDA ANDA214870 Sandoz Inc. METHYLPREDNISOLONE ACETATE 80 mg/mL 1 VIAL, MULTI-DOSE in 1 CARTON (0781-3516-75) / 5 mL in 1 VIAL, MULTI-DOSE
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