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
70771-1168-3	70771-1168	HUMAN PRESCRIPTION DRUG	fesoterodine fumarate	fesoterodine fumarate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20171207	N/A	ANDA	ANDA204946	Zydus Lifesciences Limited	FESOTERODINE FUMARATE	4 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1168-3)
70771-1168-4	70771-1168	HUMAN PRESCRIPTION DRUG	fesoterodine fumarate	fesoterodine fumarate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20171207	N/A	ANDA	ANDA204946	Zydus Lifesciences Limited	FESOTERODINE FUMARATE	4 mg/1	10 BLISTER PACK in 1 CARTON (70771-1168-4) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70771-1168-2)
70771-1168-9	70771-1168	HUMAN PRESCRIPTION DRUG	fesoterodine fumarate	fesoterodine fumarate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20171207	N/A	ANDA	ANDA204946	Zydus Lifesciences Limited	FESOTERODINE FUMARATE	4 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1168-9)
70771-1169-3	70771-1169	HUMAN PRESCRIPTION DRUG	fesoterodine fumarate	fesoterodine fumarate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20171207	N/A	ANDA	ANDA204946	Zydus Lifesciences Limited	FESOTERODINE FUMARATE	8 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1169-3)
70771-1169-4	70771-1169	HUMAN PRESCRIPTION DRUG	fesoterodine fumarate	fesoterodine fumarate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20171207	N/A	ANDA	ANDA204946	Zydus Lifesciences Limited	FESOTERODINE FUMARATE	8 mg/1	10 BLISTER PACK in 1 CARTON (70771-1169-4) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70771-1169-2)
70771-1169-9	70771-1169	HUMAN PRESCRIPTION DRUG	fesoterodine fumarate	fesoterodine fumarate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20171207	N/A	ANDA	ANDA204946	Zydus Lifesciences Limited	FESOTERODINE FUMARATE	8 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1169-9)
68382-479-06	68382-479	HUMAN PRESCRIPTION DRUG	fesoterodine fumarate	fesoterodine fumarate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20171207	N/A	ANDA	ANDA204946	Zydus Pharmaceuticals USA Inc.	FESOTERODINE FUMARATE	4 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-479-06)
68382-479-16	68382-479	HUMAN PRESCRIPTION DRUG	fesoterodine fumarate	fesoterodine fumarate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20171207	N/A	ANDA	ANDA204946	Zydus Pharmaceuticals USA Inc.	FESOTERODINE FUMARATE	4 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-479-16)
68382-479-77	68382-479	HUMAN PRESCRIPTION DRUG	fesoterodine fumarate	fesoterodine fumarate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20171207	N/A	ANDA	ANDA204946	Zydus Pharmaceuticals USA Inc.	FESOTERODINE FUMARATE	4 mg/1	10 BLISTER PACK in 1 CARTON (68382-479-77) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68382-479-30)
68382-480-06	68382-480	HUMAN PRESCRIPTION DRUG	fesoterodine fumarate	fesoterodine fumarate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20171207	N/A	ANDA	ANDA204946	Zydus Pharmaceuticals USA Inc.	FESOTERODINE FUMARATE	8 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-480-06)
68382-480-16	68382-480	HUMAN PRESCRIPTION DRUG	fesoterodine fumarate	fesoterodine fumarate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20171207	N/A	ANDA	ANDA204946	Zydus Pharmaceuticals USA Inc.	FESOTERODINE FUMARATE	8 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-480-16)
68382-480-77	68382-480	HUMAN PRESCRIPTION DRUG	fesoterodine fumarate	fesoterodine fumarate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20171207	N/A	ANDA	ANDA204946	Zydus Pharmaceuticals USA Inc.	FESOTERODINE FUMARATE	8 mg/1	10 BLISTER PACK in 1 CARTON (68382-480-77) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68382-480-30)