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=NDA014602"
符合检索条件的记录共 2 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
51754-5060-1 51754-5060 HUMAN PRESCRIPTION DRUG Betamethasone Sodium Phosphate and Betamethasone Acetate Betamethasone Sodium Phosphate and Betamethasone Acetate INJECTION, SUSPENSION INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; SOFT TISSUE 20210601 N/A NDA AUTHORIZED GENERIC NDA014602 Exela Pharma Sciences, LLC BETAMETHASONE ACETATE; BETAMETHASONE SODIUM PHOSPHATE 3 mg/mL; 3 mg/mL 1 VIAL, MULTI-DOSE in 1 BOX (51754-5060-1) / 5 mL in 1 VIAL, MULTI-DOSE
78206-118-01 78206-118 HUMAN PRESCRIPTION DRUG CELESTONE SOLUSPAN Betamethasone Acetate and Betamethasone Sodium Phosphate INJECTION, SUSPENSION INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; SOFT TISSUE 20210601 N/A NDA NDA014602 Organon LLC BETAMETHASONE ACETATE; BETAMETHASONE SODIUM PHOSPHATE 3 mg/mL; 3 mg/mL 1 VIAL, MULTI-DOSE in 1 BOX (78206-118-01) / 5 mL in 1 VIAL, MULTI-DOSE
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