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=ANDA218289"
符合检索条件的记录共 5 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
59651-699-14 59651-699 HUMAN PRESCRIPTION DRUG BETAMETHASONE DIPROPIONATE BETAMETHASONE DIPROPIONATE OINTMENT, AUGMENTED TOPICAL 20240410 N/A ANDA ANDA218289 Aurobindo Pharma Limited BETAMETHASONE DIPROPIONATE .5 mg/g 1 TUBE in 1 CARTON (59651-699-14) / 15 g in 1 TUBE
59651-699-46 59651-699 HUMAN PRESCRIPTION DRUG BETAMETHASONE DIPROPIONATE BETAMETHASONE DIPROPIONATE OINTMENT, AUGMENTED TOPICAL 20240410 N/A ANDA ANDA218289 Aurobindo Pharma Limited BETAMETHASONE DIPROPIONATE .5 mg/g 1 TUBE in 1 CARTON (59651-699-46) / 45 g in 1 TUBE
59651-699-50 59651-699 HUMAN PRESCRIPTION DRUG BETAMETHASONE DIPROPIONATE BETAMETHASONE DIPROPIONATE OINTMENT, AUGMENTED TOPICAL 20240410 N/A ANDA ANDA218289 Aurobindo Pharma Limited BETAMETHASONE DIPROPIONATE .5 mg/g 1 TUBE in 1 CARTON (59651-699-50) / 50 g in 1 TUBE
35573-107-15 35573-107 HUMAN PRESCRIPTION DRUG BETAMETHASONE DIPROPIONATE BETAMETHASONE DIPROPIONATE OINTMENT, AUGMENTED TOPICAL 20250115 N/A ANDA ANDA218289 Burel Pharmaceuticals, LLC BETAMETHASONE DIPROPIONATE .5 mg/g 1 TUBE in 1 CARTON (35573-107-15) / 15 g in 1 TUBE
35573-107-49 35573-107 HUMAN PRESCRIPTION DRUG BETAMETHASONE DIPROPIONATE BETAMETHASONE DIPROPIONATE OINTMENT, AUGMENTED TOPICAL 20250115 N/A ANDA ANDA218289 Burel Pharmaceuticals, LLC BETAMETHASONE DIPROPIONATE .5 mg/g 1 TUBE in 1 CARTON (35573-107-49) / 50 g in 1 TUBE
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