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）

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
0078-0182-01	0078-0182	HUMAN PRESCRIPTION DRUG	Sandostatin	octreotide acetate	INJECTION, SOLUTION	INTRAVENOUS; SUBCUTANEOUS	19881021	N/A	NDA	NDA019667	Novartis Pharmaceuticals Corporation	OCTREOTIDE ACETATE	500 ug/mL	10 AMPULE in 1 PACKAGE (0078-0182-01) / 1 mL in 1 AMPULE (0078-0182-61)
0078-0180-01	0078-0180	HUMAN PRESCRIPTION DRUG	Sandostatin	octreotide acetate	INJECTION, SOLUTION	INTRAVENOUS; SUBCUTANEOUS	19881021	N/A	NDA	NDA019667	Novartis Pharmaceuticals Corporation	OCTREOTIDE ACETATE	50 ug/mL	10 AMPULE in 1 PACKAGE (0078-0180-01) / 1 mL in 1 AMPULE (0078-0180-61)
0078-0181-01	0078-0181	HUMAN PRESCRIPTION DRUG	Sandostatin	octreotide acetate	INJECTION, SOLUTION	INTRAVENOUS; SUBCUTANEOUS	19881021	N/A	NDA	NDA019667	Novartis Pharmaceuticals Corporation	OCTREOTIDE ACETATE	100 ug/mL	10 AMPULE in 1 PACKAGE (0078-0181-01) / 1 mL in 1 AMPULE (0078-0181-61)