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
72888-182-30	72888-182	HUMAN PRESCRIPTION DRUG	buprenorphine hydrochloride	buprenorphine hydrochloride	TABLET	SUBLINGUAL	20240123	N/A	ANDA	ANDA090279	Advagen Pharma Ltd	BUPRENORPHINE HYDROCHLORIDE	2 mg/1	30 TABLET in 1 BOTTLE (72888-182-30)
72888-182-90	72888-182	HUMAN PRESCRIPTION DRUG	buprenorphine hydrochloride	buprenorphine hydrochloride	TABLET	SUBLINGUAL	20240123	N/A	ANDA	ANDA090279	Advagen Pharma Ltd	BUPRENORPHINE HYDROCHLORIDE	2 mg/1	90 TABLET in 1 BOTTLE (72888-182-90)
72888-183-30	72888-183	HUMAN PRESCRIPTION DRUG	buprenorphine hydrochloride	buprenorphine hydrochloride	TABLET	SUBLINGUAL	20240123	N/A	ANDA	ANDA090279	Advagen Pharma Ltd	BUPRENORPHINE HYDROCHLORIDE	8 mg/1	30 TABLET in 1 BOTTLE (72888-183-30)
72888-183-90	72888-183	HUMAN PRESCRIPTION DRUG	buprenorphine hydrochloride	buprenorphine hydrochloride	TABLET	SUBLINGUAL	20240123	N/A	ANDA	ANDA090279	Advagen Pharma Ltd	BUPRENORPHINE HYDROCHLORIDE	8 mg/1	90 TABLET in 1 BOTTLE (72888-183-90)