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
68071-3777-6	68071-3777	HUMAN PRESCRIPTION DRUG	tadalafil	tadalafil	TABLET, FILM COATED	ORAL	20250421	N/A	ANDA	ANDA209250	NuCare Pharmaceuticals,Inc.	TADALAFIL	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-3777-6)
71335-2583-2	71335-2583	HUMAN PRESCRIPTION DRUG	tadalafil	tadalafil	TABLET, FILM COATED	ORAL	20250403	N/A	ANDA	ANDA209250	Bryant Ranch Prepack	TADALAFIL	20 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (71335-2583-2)
71335-2583-3	71335-2583	HUMAN PRESCRIPTION DRUG	tadalafil	tadalafil	TABLET, FILM COATED	ORAL	20250403	N/A	ANDA	ANDA209250	Bryant Ranch Prepack	TADALAFIL	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-2583-3)
71335-2583-4	71335-2583	HUMAN PRESCRIPTION DRUG	tadalafil	tadalafil	TABLET, FILM COATED	ORAL	20250403	N/A	ANDA	ANDA209250	Bryant Ranch Prepack	TADALAFIL	20 mg/1	5 TABLET, FILM COATED in 1 BOTTLE (71335-2583-4)