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
71610-477-02	71610-477	HUMAN PRESCRIPTION DRUG	VARDENAFIL	VARDENAFIL	TABLET, FILM COATED	ORAL	20201105	N/A	ANDA	ANDA208960	Aphena Pharma Solutions - Tennessee, LLC	VARDENAFIL HYDROCHLORIDE TRIHYDRATE	20 mg/1	2 TABLET, FILM COATED in 1 BOTTLE (71610-477-02)
71610-477-04	71610-477	HUMAN PRESCRIPTION DRUG	VARDENAFIL	VARDENAFIL	TABLET, FILM COATED	ORAL	20201023	N/A	ANDA	ANDA208960	Aphena Pharma Solutions - Tennessee, LLC	VARDENAFIL HYDROCHLORIDE TRIHYDRATE	20 mg/1	4 TABLET, FILM COATED in 1 BOTTLE (71610-477-04)
71610-477-06	71610-477	HUMAN PRESCRIPTION DRUG	VARDENAFIL	VARDENAFIL	TABLET, FILM COATED	ORAL	20210503	N/A	ANDA	ANDA208960	Aphena Pharma Solutions - Tennessee, LLC	VARDENAFIL HYDROCHLORIDE TRIHYDRATE	20 mg/1	6 TABLET, FILM COATED in 1 BOTTLE (71610-477-06)
71610-477-12	71610-477	HUMAN PRESCRIPTION DRUG	VARDENAFIL	VARDENAFIL	TABLET, FILM COATED	ORAL	20210407	N/A	ANDA	ANDA208960	Aphena Pharma Solutions - Tennessee, LLC	VARDENAFIL HYDROCHLORIDE TRIHYDRATE	20 mg/1	12 TABLET, FILM COATED in 1 BOTTLE (71610-477-12)
70771-1050-1	70771-1050	HUMAN PRESCRIPTION DRUG	VARDENAFIL	VARDENAFIL	TABLET, FILM COATED	ORAL	20181101	N/A	ANDA	ANDA208960	Zydus Lifesciences Limited	VARDENAFIL HYDROCHLORIDE TRIHYDRATE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70771-1050-1)
70771-1050-3	70771-1050	HUMAN PRESCRIPTION DRUG	VARDENAFIL	VARDENAFIL	TABLET, FILM COATED	ORAL	20181101	N/A	ANDA	ANDA208960	Zydus Lifesciences Limited	VARDENAFIL HYDROCHLORIDE TRIHYDRATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70771-1050-3)
70771-1050-9	70771-1050	HUMAN PRESCRIPTION DRUG	VARDENAFIL	VARDENAFIL	TABLET, FILM COATED	ORAL	20181101	N/A	ANDA	ANDA208960	Zydus Lifesciences Limited	VARDENAFIL HYDROCHLORIDE TRIHYDRATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (70771-1050-9)
70771-1049-1	70771-1049	HUMAN PRESCRIPTION DRUG	VARDENAFIL	VARDENAFIL	TABLET, FILM COATED	ORAL	20181101	N/A	ANDA	ANDA208960	Zydus Lifesciences Limited	VARDENAFIL HYDROCHLORIDE TRIHYDRATE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70771-1049-1)
70771-1049-3	70771-1049	HUMAN PRESCRIPTION DRUG	VARDENAFIL	VARDENAFIL	TABLET, FILM COATED	ORAL	20181101	N/A	ANDA	ANDA208960	Zydus Lifesciences Limited	VARDENAFIL HYDROCHLORIDE TRIHYDRATE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70771-1049-3)
70771-1049-9	70771-1049	HUMAN PRESCRIPTION DRUG	VARDENAFIL	VARDENAFIL	TABLET, FILM COATED	ORAL	20181101	N/A	ANDA	ANDA208960	Zydus Lifesciences Limited	VARDENAFIL HYDROCHLORIDE TRIHYDRATE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (70771-1049-9)
70771-1048-1	70771-1048	HUMAN PRESCRIPTION DRUG	VARDENAFIL	VARDENAFIL	TABLET, FILM COATED	ORAL	20181101	N/A	ANDA	ANDA208960	Zydus Lifesciences Limited	VARDENAFIL HYDROCHLORIDE TRIHYDRATE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70771-1048-1)
70771-1048-3	70771-1048	HUMAN PRESCRIPTION DRUG	VARDENAFIL	VARDENAFIL	TABLET, FILM COATED	ORAL	20181101	N/A	ANDA	ANDA208960	Zydus Lifesciences Limited	VARDENAFIL HYDROCHLORIDE TRIHYDRATE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70771-1048-3)
70771-1048-9	70771-1048	HUMAN PRESCRIPTION DRUG	VARDENAFIL	VARDENAFIL	TABLET, FILM COATED	ORAL	20181101	N/A	ANDA	ANDA208960	Zydus Lifesciences Limited	VARDENAFIL HYDROCHLORIDE TRIHYDRATE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (70771-1048-9)
70771-1047-1	70771-1047	HUMAN PRESCRIPTION DRUG	VARDENAFIL	VARDENAFIL	TABLET, FILM COATED	ORAL	20181101	N/A	ANDA	ANDA208960	Zydus Lifesciences Limited	VARDENAFIL HYDROCHLORIDE TRIHYDRATE	2.5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70771-1047-1)
70771-1047-3	70771-1047	HUMAN PRESCRIPTION DRUG	VARDENAFIL	VARDENAFIL	TABLET, FILM COATED	ORAL	20181101	N/A	ANDA	ANDA208960	Zydus Lifesciences Limited	VARDENAFIL HYDROCHLORIDE TRIHYDRATE	2.5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70771-1047-3)
70771-1047-9	70771-1047	HUMAN PRESCRIPTION DRUG	VARDENAFIL	VARDENAFIL	TABLET, FILM COATED	ORAL	20181101	N/A	ANDA	ANDA208960	Zydus Lifesciences Limited	VARDENAFIL HYDROCHLORIDE TRIHYDRATE	2.5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (70771-1047-9)
70710-1068-1	70710-1068	HUMAN PRESCRIPTION DRUG	VARDENAFIL	VARDENAFIL	TABLET, FILM COATED	ORAL	20181101	N/A	ANDA	ANDA208960	Zydus Pharmaceuticals USA Inc.	VARDENAFIL HYDROCHLORIDE TRIHYDRATE	2.5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70710-1068-1)
70710-1068-3	70710-1068	HUMAN PRESCRIPTION DRUG	VARDENAFIL	VARDENAFIL	TABLET, FILM COATED	ORAL	20181101	N/A	ANDA	ANDA208960	Zydus Pharmaceuticals USA Inc.	VARDENAFIL HYDROCHLORIDE TRIHYDRATE	2.5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70710-1068-3)
70710-1068-9	70710-1068	HUMAN PRESCRIPTION DRUG	VARDENAFIL	VARDENAFIL	TABLET, FILM COATED	ORAL	20181101	N/A	ANDA	ANDA208960	Zydus Pharmaceuticals USA Inc.	VARDENAFIL HYDROCHLORIDE TRIHYDRATE	2.5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (70710-1068-9)
70710-1069-1	70710-1069	HUMAN PRESCRIPTION DRUG	VARDENAFIL	VARDENAFIL	TABLET, FILM COATED	ORAL	20181101	N/A	ANDA	ANDA208960	Zydus Pharmaceuticals USA Inc.	VARDENAFIL HYDROCHLORIDE TRIHYDRATE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70710-1069-1)