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)
检索条件:" 注册申请号=ANDA078503"
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
42291-634-01 42291-634 HUMAN PRESCRIPTION DRUG Oxybutynin Chloride Extended Release Oxybutynin Chloride TABLET, EXTENDED RELEASE ORAL 20160309 N/A ANDA ANDA078503 AvKARE OXYBUTYNIN CHLORIDE 10 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (42291-634-01)
42291-634-50 42291-634 HUMAN PRESCRIPTION DRUG Oxybutynin Chloride Extended Release Oxybutynin Chloride TABLET, EXTENDED RELEASE ORAL 20160309 N/A ANDA ANDA078503 AvKARE OXYBUTYNIN CHLORIDE 10 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (42291-634-50)
42291-635-01 42291-635 HUMAN PRESCRIPTION DRUG Oxybutynin Chloride Extended Release Oxybutynin Chloride TABLET, EXTENDED RELEASE ORAL 20160309 N/A ANDA ANDA078503 AvKARE OXYBUTYNIN CHLORIDE 15 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (42291-635-01)
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)
62135-509-90 62135-509 HUMAN PRESCRIPTION DRUG oxybutynin chloride OXYBUTYNIN CHLORIDE TABLET, EXTENDED RELEASE ORAL 20230303 N/A ANDA ANDA078503 Chartwell RX, LLC OXYBUTYNIN CHLORIDE 15 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (62135-509-90)
62135-507-90 62135-507 HUMAN PRESCRIPTION DRUG oxybutynin chloride OXYBUTYNIN CHLORIDE TABLET, EXTENDED RELEASE ORAL 20230303 N/A ANDA ANDA078503 Chartwell RX, LLC OXYBUTYNIN CHLORIDE 5 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (62135-507-90)
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)
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)
62175-270-37 62175-270 HUMAN PRESCRIPTION DRUG Oxybutynin Chloride Extended Release Oxybutynin Chloride TABLET, EXTENDED RELEASE ORAL 20090301 N/A ANDA ANDA078503 Lannett Company, Inc. OXYBUTYNIN CHLORIDE 5 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62175-270-37)
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)
62175-270-41 62175-270 HUMAN PRESCRIPTION DRUG Oxybutynin Chloride Extended Release Oxybutynin Chloride TABLET, EXTENDED RELEASE ORAL 20090301 N/A ANDA ANDA078503 Lannett Company, Inc. OXYBUTYNIN CHLORIDE 5 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (62175-270-41)
62175-271-37 62175-271 HUMAN PRESCRIPTION DRUG Oxybutynin Chloride Extended Release Oxybutynin Chloride TABLET, EXTENDED RELEASE ORAL 20090301 N/A ANDA ANDA078503 Lannett Company, Inc. OXYBUTYNIN CHLORIDE 10 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62175-271-37)
43353-282-30 43353-282 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 (43353-282-30)
43353-282-53 43353-282 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 (43353-282-53)
43353-282-60 43353-282 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 (43353-282-60)
43353-282-80 43353-282 HUMAN PRESCRIPTION DRUG Oxybutynin Chloride Extended Release Oxybutynin Chloride TABLET, EXTENDED RELEASE ORAL 20230531 N/A ANDA ANDA078503 Aphena Pharma Solutions - Tennessee, LLC OXYBUTYNIN CHLORIDE 5 mg/1 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (43353-282-80)
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)
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)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase