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
0409-1215-01	0409-1215	HUMAN PRESCRIPTION DRUG	Naloxone Hydrochloride	NALOXONE HYDROCHLORIDE	INJECTION, SOLUTION	INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS	20050712	N/A	ANDA	ANDA070256	Hospira, Inc.	NALOXONE HYDROCHLORIDE	.4 mg/mL	10 VIAL, SINGLE-DOSE in 1 CARTON (0409-1215-01) / 1 mL in 1 VIAL, SINGLE-DOSE (0409-1215-21)
51662-1242-1	51662-1242	HUMAN PRESCRIPTION DRUG	NALOXONE HCI	NALOXONE HCI	INJECTION, SOLUTION	INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS	20180818	N/A	ANDA	ANDA070256	HF Acquisition Co. LLC, DBA Health First	NALOXONE HYDROCHLORIDE	.4 mg/mL	1 mL in 1 VIAL (51662-1242-1)
51662-1242-3	51662-1242	HUMAN PRESCRIPTION DRUG	NALOXONE HCI	NALOXONE HCI	INJECTION, SOLUTION	INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS	20200615	N/A	ANDA	ANDA070256	HF Acquisition Co. LLC, DBA Health First	NALOXONE HYDROCHLORIDE	.4 mg/mL	50 POUCH in 1 CASE (51662-1242-3) / 1 mL in 1 POUCH (51662-1242-2)