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=ANDA201835"
符合检索条件的记录共 3 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
25021-821-05 25021-821 HUMAN PRESCRIPTION DRUG methylprednisolone acetate methylprednisolone acetate INJECTION, SUSPENSION INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; INTRASYNOVIAL; SOFT TISSUE 20211115 N/A ANDA ANDA201835 Sagent Pharmaceuticals METHYLPREDNISOLONE ACETATE 80 mg/mL 1 VIAL in 1 CARTON (25021-821-05) / 5 mL in 1 VIAL
25021-820-10 25021-820 HUMAN PRESCRIPTION DRUG methylprednisolone acetate methylprednisolone acetate INJECTION, SUSPENSION INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; INTRASYNOVIAL; SOFT TISSUE 20211115 N/A ANDA ANDA201835 Sagent Pharmaceuticals METHYLPREDNISOLONE ACETATE 40 mg/mL 1 VIAL in 1 CARTON (25021-820-10) / 10 mL in 1 VIAL
25021-820-05 25021-820 HUMAN PRESCRIPTION DRUG methylprednisolone acetate methylprednisolone acetate INJECTION, SUSPENSION INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; INTRASYNOVIAL; SOFT TISSUE 20211115 N/A ANDA ANDA201835 Sagent Pharmaceuticals METHYLPREDNISOLONE ACETATE 40 mg/mL 1 VIAL in 1 CARTON (25021-820-05) / 5 mL in 1 VIAL
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