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
0310-6001-30	0310-6001	HUMAN PRESCRIPTION DRUG	BAXFENDY	baxdrostat	TABLET, FILM COATED	ORAL	20260515	N/A	NDA	NDA219878	AstraZeneca Pharmaceuticals LP	BAXDROSTAT	1 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0310-6001-30)
0310-6001-95	0310-6001	HUMAN PRESCRIPTION DRUG	BAXFENDY	baxdrostat	TABLET, FILM COATED	ORAL	20260515	N/A	NDA	NDA219878	AstraZeneca Pharmaceuticals LP	BAXDROSTAT	1 mg/1	7 TABLET, FILM COATED in 1 BOTTLE (0310-6001-95)
0310-6002-30	0310-6002	HUMAN PRESCRIPTION DRUG	BAXFENDY	baxdrostat	TABLET, FILM COATED	ORAL	20260515	N/A	NDA	NDA219878	AstraZeneca Pharmaceuticals LP	BAXDROSTAT	2 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0310-6002-30)
0310-6002-95	0310-6002	HUMAN PRESCRIPTION DRUG	BAXFENDY	baxdrostat	TABLET, FILM COATED	ORAL	20260515	N/A	NDA	NDA219878	AstraZeneca Pharmaceuticals LP	BAXDROSTAT	2 mg/1	7 TABLET, FILM COATED in 1 BOTTLE (0310-6002-95)