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=ANDA075957"
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
71288-566-02 71288-566 HUMAN PRESCRIPTION DRUG Octreotide Acetate Octreotide Acetate INJECTION, SOLUTION INTRAVENOUS; SUBCUTANEOUS 20250228 N/A ANDA ANDA075957 Meitheal Pharmaceuticals, Inc. OCTREOTIDE ACETATE 50 ug/mL 10 VIAL, SINGLE-DOSE in 1 CARTON (71288-566-02) / 1 mL in 1 VIAL, SINGLE-DOSE (71288-566-01)
71288-568-02 71288-568 HUMAN PRESCRIPTION DRUG Octreotide Acetate Octreotide Acetate INJECTION, SOLUTION INTRAVENOUS; SUBCUTANEOUS 20250228 N/A ANDA ANDA075957 Meitheal Pharmaceuticals, Inc. OCTREOTIDE ACETATE 500 ug/mL 10 VIAL, SINGLE-DOSE in 1 CARTON (71288-568-02) / 1 mL in 1 VIAL, SINGLE-DOSE (71288-568-01)
71288-567-02 71288-567 HUMAN PRESCRIPTION DRUG Octreotide Acetate Octreotide Acetate INJECTION, SOLUTION INTRAVENOUS; SUBCUTANEOUS 20250228 N/A ANDA ANDA075957 Meitheal Pharmaceuticals, Inc. OCTREOTIDE ACETATE 100 ug/mL 10 VIAL, SINGLE-DOSE in 1 CARTON (71288-567-02) / 1 mL in 1 VIAL, SINGLE-DOSE (71288-567-01)
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