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=ANDA065131"
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
49884-511-01 49884-511 HUMAN PRESCRIPTION DRUG Minocycline Minocycline TABLET ORAL 20030416 N/A ANDA ANDA065131 Par Pharmaceutical, Inc. MINOCYCLINE HYDROCHLORIDE 50 mg/1 100 TABLET in 1 BOTTLE (49884-511-01)
49884-512-01 49884-512 HUMAN PRESCRIPTION DRUG Minocycline Minocycline TABLET ORAL 20030416 N/A ANDA ANDA065131 Par Pharmaceutical, Inc. MINOCYCLINE HYDROCHLORIDE 75 mg/1 100 TABLET in 1 BOTTLE (49884-512-01)
49884-513-03 49884-513 HUMAN PRESCRIPTION DRUG Minocycline Minocycline TABLET ORAL 20030416 N/A ANDA ANDA065131 Par Pharmaceutical, Inc. MINOCYCLINE HYDROCHLORIDE 100 mg/1 50 TABLET in 1 BOTTLE (49884-513-03)
64380-155-01 64380-155 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET ORAL 20220411 N/A ANDA ANDA065131 Strides Pharma Science Limited MINOCYCLINE HYDROCHLORIDE 75 mg/1 100 TABLET in 1 BOTTLE (64380-155-01)
64380-156-01 64380-156 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET ORAL 20220411 N/A ANDA ANDA065131 Strides Pharma Science Limited MINOCYCLINE HYDROCHLORIDE 100 mg/1 50 TABLET in 1 BOTTLE (64380-156-01)
42291-591-60 42291-591 HUMAN PRESCRIPTION DRUG Minocycline Minocycline TABLET ORAL 20150508 N/A ANDA ANDA065131 AvKARE MINOCYCLINE HYDROCHLORIDE 100 mg/1 60 TABLET in 1 BOTTLE (42291-591-60)
42291-589-90 42291-589 HUMAN PRESCRIPTION DRUG Minocycline Minocycline TABLET ORAL 20150508 N/A ANDA ANDA065131 AvKARE MINOCYCLINE HYDROCHLORIDE 50 mg/1 90 TABLET in 1 BOTTLE (42291-589-90)
64380-154-01 64380-154 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET ORAL 20220411 N/A ANDA ANDA065131 Strides Pharma Science Limited MINOCYCLINE HYDROCHLORIDE 50 mg/1 100 TABLET in 1 BOTTLE (64380-154-01)
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