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=ANDA079087"
符合检索条件的记录共 56 条，共 3 页，当前第 2 页 ，可点击列名称排序
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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
0115-1233-13 0115-1233 HUMAN PRESCRIPTION DRUG Oxymorphone hydrochloride Oxymorphone hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20130102 N/A ANDA ANDA079087 Amneal Pharmaceuticals of New York LLC OXYMORPHONE HYDROCHLORIDE 20 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1233-13)
0115-1317-01 0115-1317 HUMAN PRESCRIPTION DRUG Oxymorphone hydrochloride Oxymorphone hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20130102 N/A ANDA ANDA079087 Amneal Pharmaceuticals of New York LLC OXYMORPHONE HYDROCHLORIDE 30 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1317-01)
0115-1317-03 0115-1317 HUMAN PRESCRIPTION DRUG Oxymorphone hydrochloride Oxymorphone hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20130102 N/A ANDA ANDA079087 Amneal Pharmaceuticals of New York LLC OXYMORPHONE HYDROCHLORIDE 30 mg/1 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1317-03)
0115-1317-08 0115-1317 HUMAN PRESCRIPTION DRUG Oxymorphone hydrochloride Oxymorphone hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20130102 N/A ANDA ANDA079087 Amneal Pharmaceuticals of New York LLC OXYMORPHONE HYDROCHLORIDE 30 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1317-08)
0115-1317-13 0115-1317 HUMAN PRESCRIPTION DRUG Oxymorphone hydrochloride Oxymorphone hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20130102 N/A ANDA ANDA079087 Amneal Pharmaceuticals of New York LLC OXYMORPHONE HYDROCHLORIDE 30 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1317-13)
64896-696-08 64896-696 HUMAN PRESCRIPTION DRUG Oxymorphone hydrochloride Oxymorphone hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20130102 N/A ANDA ANDA079087 Amneal Pharmaceuticals LLC OXYMORPHONE HYDROCHLORIDE 7.5 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-696-08)
64896-696-13 64896-696 HUMAN PRESCRIPTION DRUG Oxymorphone hydrochloride Oxymorphone hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20130102 N/A ANDA ANDA079087 Amneal Pharmaceuticals LLC OXYMORPHONE HYDROCHLORIDE 7.5 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-696-13)
64896-696-01 64896-696 HUMAN PRESCRIPTION DRUG Oxymorphone hydrochloride Oxymorphone hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20130102 N/A ANDA ANDA079087 Amneal Pharmaceuticals LLC OXYMORPHONE HYDROCHLORIDE 7.5 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-696-01)
64896-696-03 64896-696 HUMAN PRESCRIPTION DRUG Oxymorphone hydrochloride Oxymorphone hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20130102 N/A ANDA ANDA079087 Amneal Pharmaceuticals LLC OXYMORPHONE HYDROCHLORIDE 7.5 mg/1 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-696-03)
64896-700-01 64896-700 HUMAN PRESCRIPTION DRUG Oxymorphone hydrochloride Oxymorphone hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20130102 N/A ANDA ANDA079087 Amneal Pharmaceuticals LLC OXYMORPHONE HYDROCHLORIDE 30 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-700-01)
64896-700-03 64896-700 HUMAN PRESCRIPTION DRUG Oxymorphone hydrochloride Oxymorphone hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20130102 N/A ANDA ANDA079087 Amneal Pharmaceuticals LLC OXYMORPHONE HYDROCHLORIDE 30 mg/1 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-700-03)
64896-700-08 64896-700 HUMAN PRESCRIPTION DRUG Oxymorphone hydrochloride Oxymorphone hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20130102 N/A ANDA ANDA079087 Amneal Pharmaceuticals LLC OXYMORPHONE HYDROCHLORIDE 30 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-700-08)
64896-700-13 64896-700 HUMAN PRESCRIPTION DRUG Oxymorphone hydrochloride Oxymorphone hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20130102 N/A ANDA ANDA079087 Amneal Pharmaceuticals LLC OXYMORPHONE HYDROCHLORIDE 30 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-700-13)
0115-1315-01 0115-1315 HUMAN PRESCRIPTION DRUG Oxymorphone hydrochloride Oxymorphone hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20130102 N/A ANDA ANDA079087 Amneal Pharmaceuticals of New York LLC OXYMORPHONE HYDROCHLORIDE 7.5 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1315-01)
0115-1315-03 0115-1315 HUMAN PRESCRIPTION DRUG Oxymorphone hydrochloride Oxymorphone hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20130102 N/A ANDA ANDA079087 Amneal Pharmaceuticals of New York LLC OXYMORPHONE HYDROCHLORIDE 7.5 mg/1 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1315-03)
0115-1315-08 0115-1315 HUMAN PRESCRIPTION DRUG Oxymorphone hydrochloride Oxymorphone hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20130102 N/A ANDA ANDA079087 Amneal Pharmaceuticals of New York LLC OXYMORPHONE HYDROCHLORIDE 7.5 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1315-08)
0115-1315-13 0115-1315 HUMAN PRESCRIPTION DRUG Oxymorphone hydrochloride Oxymorphone hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20130102 N/A ANDA ANDA079087 Amneal Pharmaceuticals of New York LLC OXYMORPHONE HYDROCHLORIDE 7.5 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1315-13)
64896-695-01 64896-695 HUMAN PRESCRIPTION DRUG Oxymorphone hydrochloride Oxymorphone hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20130102 N/A ANDA ANDA079087 Amneal Pharmaceuticals LLC OXYMORPHONE HYDROCHLORIDE 5 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-695-01)
64896-695-03 64896-695 HUMAN PRESCRIPTION DRUG Oxymorphone hydrochloride Oxymorphone hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20130102 N/A ANDA ANDA079087 Amneal Pharmaceuticals LLC OXYMORPHONE HYDROCHLORIDE 5 mg/1 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-695-03)
64896-695-08 64896-695 HUMAN PRESCRIPTION DRUG Oxymorphone hydrochloride Oxymorphone hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20130102 N/A ANDA ANDA079087 Amneal Pharmaceuticals LLC OXYMORPHONE HYDROCHLORIDE 5 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-695-08)
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