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=ANDA202261"
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
65862-554-01 65862-554 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20121119 N/A ANDA ANDA202261 Aurobindo Pharma Limited MINOCYCLINE HYDROCHLORIDE 45 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-554-01)
65862-554-30 65862-554 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20121119 N/A ANDA ANDA202261 Aurobindo Pharma Limited MINOCYCLINE HYDROCHLORIDE 45 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-554-30)
65862-554-99 65862-554 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20121119 N/A ANDA ANDA202261 Aurobindo Pharma Limited MINOCYCLINE HYDROCHLORIDE 45 mg/1 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-554-99)
65862-557-30 65862-557 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180928 N/A ANDA ANDA202261 Aurobindo Pharma Limited MINOCYCLINE HYDROCHLORIDE 115 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-557-30)
65862-557-99 65862-557 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180928 N/A ANDA ANDA202261 Aurobindo Pharma Limited MINOCYCLINE HYDROCHLORIDE 115 mg/1 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-557-99)
65862-885-01 65862-885 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20160613 N/A ANDA ANDA202261 Aurobindo Pharma Limited MINOCYCLINE HYDROCHLORIDE 105 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-885-01)
65862-885-05 65862-885 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20160613 N/A ANDA ANDA202261 Aurobindo Pharma Limited MINOCYCLINE HYDROCHLORIDE 105 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-885-05)
65862-885-30 65862-885 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20160613 N/A ANDA ANDA202261 Aurobindo Pharma Limited MINOCYCLINE HYDROCHLORIDE 105 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-885-30)
65862-885-99 65862-885 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20160613 N/A ANDA ANDA202261 Aurobindo Pharma Limited MINOCYCLINE HYDROCHLORIDE 105 mg/1 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-885-99)
42546-777-30 42546-777 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20121119 N/A ANDA ANDA202261 PruGen Pharmaceuticals MINOCYCLINE HYDROCHLORIDE 135 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42546-777-30)
65862-556-01 65862-556 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20121119 N/A ANDA ANDA202261 Aurobindo Pharma Limited MINOCYCLINE HYDROCHLORIDE 90 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-556-01)
65862-556-30 65862-556 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20121119 N/A ANDA ANDA202261 Aurobindo Pharma Limited MINOCYCLINE HYDROCHLORIDE 90 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-556-30)
65862-556-99 65862-556 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20121119 N/A ANDA ANDA202261 Aurobindo Pharma Limited MINOCYCLINE HYDROCHLORIDE 90 mg/1 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-556-99)
65862-884-01 65862-884 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20160613 N/A ANDA ANDA202261 Aurobindo Pharma Limited MINOCYCLINE HYDROCHLORIDE 80 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-884-01)
65862-884-05 65862-884 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20160613 N/A ANDA ANDA202261 Aurobindo Pharma Limited MINOCYCLINE HYDROCHLORIDE 80 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-884-05)
65862-884-30 65862-884 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20160613 N/A ANDA ANDA202261 Aurobindo Pharma Limited MINOCYCLINE HYDROCHLORIDE 80 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-884-30)
65862-884-99 65862-884 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20160613 N/A ANDA ANDA202261 Aurobindo Pharma Limited MINOCYCLINE HYDROCHLORIDE 80 mg/1 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-884-99)
42546-774-30 42546-774 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20121119 N/A ANDA ANDA202261 PruGen Pharmaceuticals MINOCYCLINE HYDROCHLORIDE 90 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42546-774-30)
65862-555-30 65862-555 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180928 N/A ANDA ANDA202261 Aurobindo Pharma Limited MINOCYCLINE HYDROCHLORIDE 65 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-555-30)
65862-555-99 65862-555 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180928 N/A ANDA ANDA202261 Aurobindo Pharma Limited MINOCYCLINE HYDROCHLORIDE 65 mg/1 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-555-99)
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