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=ANDA075883"
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
70518-3619-0 70518-3619 HUMAN PRESCRIPTION DRUG Ammonium Lactate Ammonium Lactate CREAM TOPICAL 20230120 N/A ANDA ANDA075883 REMEDYREPACK INC. AMMONIUM LACTATE 120 mg/g 2 TUBE in 1 CARTON (70518-3619-0) / 140 g in 1 TUBE
51672-1301-4 51672-1301 HUMAN PRESCRIPTION DRUG Ammonium Lactate Ammonium Lactate CREAM TOPICAL 20030410 N/A ANDA ANDA075883 Sun Pharmaceutical Industries, Inc. AMMONIUM LACTATE 120 mg/g 2 TUBE in 1 CARTON (51672-1301-4) / 140 g in 1 TUBE
51672-1301-2 51672-1301 HUMAN PRESCRIPTION DRUG Ammonium Lactate Ammonium Lactate CREAM TOPICAL 20240701 N/A ANDA ANDA075883 Sun Pharmaceutical Industries, Inc. AMMONIUM LACTATE 120 mg/g 1 TUBE in 1 CARTON (51672-1301-2) / 140 g in 1 TUBE
51672-1301-0 51672-1301 HUMAN PRESCRIPTION DRUG Ammonium Lactate Ammonium Lactate CREAM TOPICAL 20030410 N/A ANDA ANDA075883 Sun Pharmaceutical Industries, Inc. AMMONIUM LACTATE 120 mg/g 385 g in 1 BOTTLE, PLASTIC (51672-1301-0)
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