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=ANDA090834"
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
25021-463-01 25021-463 HUMAN PRESCRIPTION DRUG Octreotide Acetate octreotide acetate INJECTION, SOLUTION INTRAVENOUS; SUBCUTANEOUS 20230615 N/A ANDA ANDA090834 Sagent Pharmaceuticals OCTREOTIDE ACETATE 50 ug/mL 10 VIAL in 1 CARTON (25021-463-01) / 1 mL in 1 VIAL
25021-464-01 25021-464 HUMAN PRESCRIPTION DRUG Octreotide Acetate octreotide acetate INJECTION, SOLUTION INTRAVENOUS; SUBCUTANEOUS 20230615 N/A ANDA ANDA090834 Sagent Pharmaceuticals OCTREOTIDE ACETATE 100 ug/mL 10 VIAL in 1 CARTON (25021-464-01) / 1 mL in 1 VIAL
25021-465-01 25021-465 HUMAN PRESCRIPTION DRUG Octreotide Acetate octreotide acetate INJECTION, SOLUTION INTRAVENOUS; SUBCUTANEOUS 20230615 N/A ANDA ANDA090834 Sagent Pharmaceuticals OCTREOTIDE ACETATE 500 ug/mL 10 VIAL in 1 CARTON (25021-465-01) / 1 mL in 1 VIAL
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