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=ANDA202332"
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
70771-1086-9 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 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1086-9)
70771-1086-6 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 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1086-6)
70771-1086-5 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/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1086-5)
70771-1087-1 70771-1087 HUMAN PRESCRIPTION DRUG oxybutynin oxybutynin TABLET, FILM COATED, EXTENDED RELEASE ORAL 20170810 N/A ANDA ANDA202332 Zydus Lifesciences Limited OXYBUTYNIN CHLORIDE 10 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1087-1)
70771-1087-3 70771-1087 HUMAN PRESCRIPTION DRUG oxybutynin oxybutynin TABLET, FILM COATED, EXTENDED RELEASE ORAL 20170810 N/A ANDA ANDA202332 Zydus Lifesciences Limited OXYBUTYNIN CHLORIDE 10 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1087-3)
70771-1087-4 70771-1087 HUMAN PRESCRIPTION DRUG oxybutynin oxybutynin TABLET, FILM COATED, EXTENDED RELEASE ORAL 20170810 N/A ANDA ANDA202332 Zydus Lifesciences Limited OXYBUTYNIN CHLORIDE 10 mg/1 10 BLISTER PACK in 1 CARTON (70771-1087-4) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70771-1087-2)
70771-1087-5 70771-1087 HUMAN PRESCRIPTION DRUG oxybutynin oxybutynin TABLET, FILM COATED, EXTENDED RELEASE ORAL 20170810 N/A ANDA ANDA202332 Zydus Lifesciences Limited OXYBUTYNIN CHLORIDE 10 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1087-5)
70771-1087-6 70771-1087 HUMAN PRESCRIPTION DRUG oxybutynin oxybutynin TABLET, FILM COATED, EXTENDED RELEASE ORAL 20170810 N/A ANDA ANDA202332 Zydus Lifesciences Limited OXYBUTYNIN CHLORIDE 10 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1087-6)
70771-1087-9 70771-1087 HUMAN PRESCRIPTION DRUG oxybutynin oxybutynin TABLET, FILM COATED, EXTENDED RELEASE ORAL 20170810 N/A ANDA ANDA202332 Zydus Lifesciences Limited OXYBUTYNIN CHLORIDE 10 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1087-9)
70771-1088-1 70771-1088 HUMAN PRESCRIPTION DRUG oxybutynin oxybutynin TABLET, FILM COATED, EXTENDED RELEASE ORAL 20170810 N/A ANDA ANDA202332 Zydus Lifesciences Limited OXYBUTYNIN CHLORIDE 15 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1088-1)
70771-1088-3 70771-1088 HUMAN PRESCRIPTION DRUG oxybutynin oxybutynin TABLET, FILM COATED, EXTENDED RELEASE ORAL 20170810 N/A ANDA ANDA202332 Zydus Lifesciences Limited OXYBUTYNIN CHLORIDE 15 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1088-3)
70771-1088-4 70771-1088 HUMAN PRESCRIPTION DRUG oxybutynin oxybutynin TABLET, FILM COATED, EXTENDED RELEASE ORAL 20170810 N/A ANDA ANDA202332 Zydus Lifesciences Limited OXYBUTYNIN CHLORIDE 15 mg/1 10 BLISTER PACK in 1 CARTON (70771-1088-4) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70771-1088-2)
70771-1088-5 70771-1088 HUMAN PRESCRIPTION DRUG oxybutynin oxybutynin TABLET, FILM COATED, EXTENDED RELEASE ORAL 20170810 N/A ANDA ANDA202332 Zydus Lifesciences Limited OXYBUTYNIN CHLORIDE 15 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1088-5)
70771-1088-6 70771-1088 HUMAN PRESCRIPTION DRUG oxybutynin oxybutynin TABLET, FILM COATED, EXTENDED RELEASE ORAL 20170810 N/A ANDA ANDA202332 Zydus Lifesciences Limited OXYBUTYNIN CHLORIDE 15 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1088-6)
70771-1088-9 70771-1088 HUMAN PRESCRIPTION DRUG oxybutynin oxybutynin TABLET, FILM COATED, EXTENDED RELEASE ORAL 20170810 N/A ANDA ANDA202332 Zydus Lifesciences Limited OXYBUTYNIN CHLORIDE 15 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1088-9)
70771-1086-4 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 10 BLISTER PACK in 1 CARTON (70771-1086-4) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70771-1086-2)
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)
0615-8219-39 0615-8219 HUMAN PRESCRIPTION DRUG oxybutynin oxybutynin TABLET, FILM COATED, EXTENDED RELEASE ORAL 20190125 N/A ANDA ANDA202332 NCS HealthCare of KY, LLC dba Vangard Labs OXYBUTYNIN CHLORIDE 5 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0615-8219-39)
0615-8220-39 0615-8220 HUMAN PRESCRIPTION DRUG oxybutynin oxybutynin TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180628 N/A ANDA ANDA202332 NCS HealthCare of KY, LLC dba Vangard Labs OXYBUTYNIN CHLORIDE 10 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0615-8220-39)
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