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
0404-9920-01	0404-9920	HUMAN PRESCRIPTION DRUG	Naloxone Hydrochloride	Naloxone Hydrochloride	INJECTION, SOLUTION	INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS	20220113	N/A	ANDA	ANDA070172	Henry Schein, Inc.	NALOXONE HYDROCHLORIDE	.4 mg/mL	1 BOX in 1 BAG (0404-9920-01) / 1 CARTRIDGE in 1 BOX / 1 mL in 1 CARTRIDGE
51662-1238-1	51662-1238	HUMAN PRESCRIPTION DRUG	NALOXONE HYDROCHLORIDE	NALOXONE HYDROCHLORIDE	INJECTION, SOLUTION	INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS	20180903	N/A	ANDA	ANDA070172	HF Acquisition Co. LLC, DBA HealthFirst	NALOXONE HYDROCHLORIDE	.4 mg/mL	1 mL in 1 CARTRIDGE (51662-1238-1)
0409-1782-69	0409-1782	HUMAN PRESCRIPTION DRUG	Naloxone Hydrochloride	NALOXONE HYDROCHLORIDE	INJECTION, SOLUTION	INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS	20050923	N/A	ANDA	ANDA070172	Hospira, Inc.	NALOXONE HYDROCHLORIDE	.4 mg/mL	10 CARTRIDGE in 1 BOX (0409-1782-69) / 1 mL in 1 CARTRIDGE (0409-1782-03)