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
43353-285-30	43353-285	HUMAN PRESCRIPTION DRUG	Oxybutynin Chloride Extended Release	Oxybutynin Chloride	TABLET, EXTENDED RELEASE	ORAL	20170302	N/A	ANDA	ANDA078503	Aphena Pharma Solutions - Tennessee, LLC	OXYBUTYNIN CHLORIDE	5 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (43353-285-30)
43353-285-53	43353-285	HUMAN PRESCRIPTION DRUG	Oxybutynin Chloride Extended Release	Oxybutynin Chloride	TABLET, EXTENDED RELEASE	ORAL	20170302	N/A	ANDA	ANDA078503	Aphena Pharma Solutions - Tennessee, LLC	OXYBUTYNIN CHLORIDE	5 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (43353-285-53)
43353-285-60	43353-285	HUMAN PRESCRIPTION DRUG	Oxybutynin Chloride Extended Release	Oxybutynin Chloride	TABLET, EXTENDED RELEASE	ORAL	20170302	N/A	ANDA	ANDA078503	Aphena Pharma Solutions - Tennessee, LLC	OXYBUTYNIN CHLORIDE	5 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (43353-285-60)
50268-629-13	50268-629	HUMAN PRESCRIPTION DRUG	Oxybutynin Chloride Extended Release	Oxybutynin Chloride	TABLET, EXTENDED RELEASE	ORAL	20120525	N/A	ANDA	ANDA078503	AvPAK	OXYBUTYNIN CHLORIDE	15 mg/1	30 BLISTER PACK in 1 BOX (50268-629-13) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (50268-629-11)
62135-508-90	62135-508	HUMAN PRESCRIPTION DRUG	oxybutynin chloride	OXYBUTYNIN CHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20230303	N/A	ANDA	ANDA078503	Chartwell RX, LLC	OXYBUTYNIN CHLORIDE	10 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (62135-508-90)
42291-633-01	42291-633	HUMAN PRESCRIPTION DRUG	Oxybutynin Chloride Extended Release	Oxybutynin Chloride	TABLET, EXTENDED RELEASE	ORAL	20160309	N/A	ANDA	ANDA078503	AvKARE	OXYBUTYNIN CHLORIDE	5 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (42291-633-01)
42291-633-50	42291-633	HUMAN PRESCRIPTION DRUG	Oxybutynin Chloride Extended Release	Oxybutynin Chloride	TABLET, EXTENDED RELEASE	ORAL	20160309	N/A	ANDA	ANDA078503	AvKARE	OXYBUTYNIN CHLORIDE	5 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (42291-633-50)
43353-284-30	43353-284	HUMAN PRESCRIPTION DRUG	Oxybutynin Chloride Extended Release	Oxybutynin Chloride	TABLET, EXTENDED RELEASE	ORAL	20171019	N/A	ANDA	ANDA078503	Aphena Pharma Solutions - Tennessee, LLC	OXYBUTYNIN CHLORIDE	10 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (43353-284-30)
43353-284-60	43353-284	HUMAN PRESCRIPTION DRUG	Oxybutynin Chloride Extended Release	Oxybutynin Chloride	TABLET, EXTENDED RELEASE	ORAL	20171019	N/A	ANDA	ANDA078503	Aphena Pharma Solutions - Tennessee, LLC	OXYBUTYNIN CHLORIDE	10 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (43353-284-60)
62175-272-37	62175-272	HUMAN PRESCRIPTION DRUG	Oxybutynin Chloride Extended Release	Oxybutynin Chloride	TABLET, EXTENDED RELEASE	ORAL	20090301	N/A	ANDA	ANDA078503	Lannett Company, Inc.	OXYBUTYNIN CHLORIDE	15 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62175-272-37)
62175-272-41	62175-272	HUMAN PRESCRIPTION DRUG	Oxybutynin Chloride Extended Release	Oxybutynin Chloride	TABLET, EXTENDED RELEASE	ORAL	20090301	N/A	ANDA	ANDA078503	Lannett Company, Inc.	OXYBUTYNIN CHLORIDE	15 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (62175-272-41)