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"
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
0115-1233-01 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/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1233-01)
0115-1233-03 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 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1233-03)
0115-1233-08 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 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1233-08)
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)
64896-698-01 64896-698 HUMAN PRESCRIPTION DRUG Oxymorphone hydrochloride Oxymorphone hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20130102 N/A ANDA ANDA079087 Amneal Pharmaceuticals LLC OXYMORPHONE HYDROCHLORIDE 15 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-698-01)
0115-1316-01 0115-1316 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 15 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1316-01)
0115-1316-03 0115-1316 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 15 mg/1 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1316-03)
0115-1316-08 0115-1316 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 15 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1316-08)
0115-1316-13 0115-1316 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 15 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1316-13)
64896-697-01 64896-697 HUMAN PRESCRIPTION DRUG Oxymorphone hydrochloride Oxymorphone hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20130102 N/A ANDA ANDA079087 Amneal Pharmaceuticals LLC OXYMORPHONE HYDROCHLORIDE 10 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-697-01)
64896-697-03 64896-697 HUMAN PRESCRIPTION DRUG Oxymorphone hydrochloride Oxymorphone hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20130102 N/A ANDA ANDA079087 Amneal Pharmaceuticals LLC OXYMORPHONE HYDROCHLORIDE 10 mg/1 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-697-03)
64896-697-08 64896-697 HUMAN PRESCRIPTION DRUG Oxymorphone hydrochloride Oxymorphone hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20130102 N/A ANDA ANDA079087 Amneal Pharmaceuticals LLC OXYMORPHONE HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-697-08)
64896-697-13 64896-697 HUMAN PRESCRIPTION DRUG Oxymorphone hydrochloride Oxymorphone hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20130102 N/A ANDA ANDA079087 Amneal Pharmaceuticals LLC OXYMORPHONE HYDROCHLORIDE 10 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-697-13)
64896-701-01 64896-701 HUMAN PRESCRIPTION DRUG Oxymorphone hydrochloride Oxymorphone hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20130102 N/A ANDA ANDA079087 Amneal Pharmaceuticals LLC OXYMORPHONE HYDROCHLORIDE 40 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-701-01)
0115-1234-01 0115-1234 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 40 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1234-01)
0115-1234-03 0115-1234 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 40 mg/1 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1234-03)
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