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
50090-5353-0	50090-5353	HUMAN PRESCRIPTION DRUG	oxybutynin	oxybutynin	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20201111	N/A	ANDA	ANDA202332	A-S Medication Solutions	OXYBUTYNIN CHLORIDE	10 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-5353-0)
68382-255-14	68382-255	HUMAN PRESCRIPTION DRUG	oxybutynin	oxybutynin	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20170810	N/A	ANDA	ANDA202332	Zydus Pharmaceuticals USA Inc.	OXYBUTYNIN CHLORIDE	5 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-255-14)
68382-255-16	68382-255	HUMAN PRESCRIPTION DRUG	oxybutynin	oxybutynin	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20170810	N/A	ANDA	ANDA202332	Zydus Pharmaceuticals USA Inc.	OXYBUTYNIN CHLORIDE	5 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-255-16)
68382-255-77	68382-255	HUMAN PRESCRIPTION DRUG	oxybutynin	oxybutynin	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20170810	N/A	ANDA	ANDA202332	Zydus Pharmaceuticals USA Inc.	OXYBUTYNIN CHLORIDE	5 mg/1	10 BLISTER PACK in 1 CARTON (68382-255-77) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68382-255-30)
68382-255-06	68382-255	HUMAN PRESCRIPTION DRUG	oxybutynin	oxybutynin	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20170810	N/A	ANDA	ANDA202332	Zydus Pharmaceuticals USA Inc.	OXYBUTYNIN CHLORIDE	5 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-255-06)
68382-255-05	68382-255	HUMAN PRESCRIPTION DRUG	oxybutynin	oxybutynin	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20170810	N/A	ANDA	ANDA202332	Zydus Pharmaceuticals USA Inc.	OXYBUTYNIN CHLORIDE	5 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-255-05)
68382-255-01	68382-255	HUMAN PRESCRIPTION DRUG	oxybutynin	oxybutynin	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20170810	N/A	ANDA	ANDA202332	Zydus Pharmaceuticals USA Inc.	OXYBUTYNIN CHLORIDE	5 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-255-01)
68382-256-01	68382-256	HUMAN PRESCRIPTION DRUG	oxybutynin	oxybutynin	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20170810	N/A	ANDA	ANDA202332	Zydus Pharmaceuticals USA Inc.	OXYBUTYNIN CHLORIDE	10 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-256-01)
68382-256-16	68382-256	HUMAN PRESCRIPTION DRUG	oxybutynin	oxybutynin	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20170810	N/A	ANDA	ANDA202332	Zydus Pharmaceuticals USA Inc.	OXYBUTYNIN CHLORIDE	10 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-256-16)
68382-256-77	68382-256	HUMAN PRESCRIPTION DRUG	oxybutynin	oxybutynin	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20170810	N/A	ANDA	ANDA202332	Zydus Pharmaceuticals USA Inc.	OXYBUTYNIN CHLORIDE	10 mg/1	10 BLISTER PACK in 1 CARTON (68382-256-77) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68382-256-30)
68382-257-01	68382-257	HUMAN PRESCRIPTION DRUG	oxybutynin	oxybutynin	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20170810	N/A	ANDA	ANDA202332	Zydus Pharmaceuticals USA Inc.	OXYBUTYNIN CHLORIDE	15 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-257-01)
68382-257-05	68382-257	HUMAN PRESCRIPTION DRUG	oxybutynin	oxybutynin	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20170810	N/A	ANDA	ANDA202332	Zydus Pharmaceuticals USA Inc.	OXYBUTYNIN CHLORIDE	15 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-257-05)
68382-257-06	68382-257	HUMAN PRESCRIPTION DRUG	oxybutynin	oxybutynin	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20170810	N/A	ANDA	ANDA202332	Zydus Pharmaceuticals USA Inc.	OXYBUTYNIN CHLORIDE	15 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-257-06)
68382-257-14	68382-257	HUMAN PRESCRIPTION DRUG	oxybutynin	oxybutynin	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20170810	N/A	ANDA	ANDA202332	Zydus Pharmaceuticals USA Inc.	OXYBUTYNIN CHLORIDE	15 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-257-14)
68382-257-16	68382-257	HUMAN PRESCRIPTION DRUG	oxybutynin	oxybutynin	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20170810	N/A	ANDA	ANDA202332	Zydus Pharmaceuticals USA Inc.	OXYBUTYNIN CHLORIDE	15 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-257-16)
68382-257-77	68382-257	HUMAN PRESCRIPTION DRUG	oxybutynin	oxybutynin	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20170810	N/A	ANDA	ANDA202332	Zydus Pharmaceuticals USA Inc.	OXYBUTYNIN CHLORIDE	15 mg/1	10 BLISTER PACK in 1 CARTON (68382-257-77) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68382-257-30)
68382-256-05	68382-256	HUMAN PRESCRIPTION DRUG	oxybutynin	oxybutynin	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20170810	N/A	ANDA	ANDA202332	Zydus Pharmaceuticals USA Inc.	OXYBUTYNIN CHLORIDE	10 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-256-05)
68382-256-06	68382-256	HUMAN PRESCRIPTION DRUG	oxybutynin	oxybutynin	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20170810	N/A	ANDA	ANDA202332	Zydus Pharmaceuticals USA Inc.	OXYBUTYNIN CHLORIDE	10 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-256-06)
70771-1086-1	70771-1086	HUMAN PRESCRIPTION DRUG	oxybutynin	oxybutynin	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20170810	N/A	ANDA	ANDA202332	Zydus Lifesciences Limited	OXYBUTYNIN CHLORIDE	5 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1086-1)
70771-1086-3	70771-1086	HUMAN PRESCRIPTION DRUG	oxybutynin	oxybutynin	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20170810	N/A	ANDA	ANDA202332	Zydus Lifesciences Limited	OXYBUTYNIN CHLORIDE	5 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1086-3)