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
65219-293-01	65219-293	HUMAN PRESCRIPTION DRUG	Desmopressin Acetate	Desmopressin Acetate	INJECTION, SOLUTION	INTRAVENOUS; SUBCUTANEOUS	20230911	N/A	ANDA	ANDA216922	Fresenius Kabi USA, LLC	DESMOPRESSIN ACETATE	4 ug/mL	10 VIAL, SINGLE-DOSE in 1 CARTON (65219-293-01) / 1 mL in 1 VIAL, SINGLE-DOSE (65219-293-00)
70095-026-02	70095-026	HUMAN PRESCRIPTION DRUG	Desmopressin Acetate	Desmopressin Acetate	INJECTION, SOLUTION	INTRAVENOUS; SUBCUTANEOUS	20230403	N/A	ANDA	ANDA216922	Sun Pharmaceutical Industries Limited	DESMOPRESSIN ACETATE	4 ug/mL	10 VIAL, SINGLE-DOSE in 1 CARTON (70095-026-02) / 1 mL in 1 VIAL, SINGLE-DOSE (70095-026-01)
68083-550-10	68083-550	HUMAN PRESCRIPTION DRUG	Desmopressin Acetate	Desmopressin Acetate	INJECTION, SOLUTION	INTRAVENOUS; SUBCUTANEOUS	20221116	N/A	ANDA	ANDA216922	Gland Pharma Limited	DESMOPRESSIN ACETATE	4 ug/mL	10 VIAL, SINGLE-DOSE in 1 CARTON (68083-550-10) / 1 mL in 1 VIAL, SINGLE-DOSE (68083-550-01)