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=ANDA204453"
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
67877-437-01 67877-437 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20160930 N/A ANDA ANDA204453 Ascend Laboratories, LLC MINOCYCLINE HYDROCHLORIDE 80 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-437-01)
67877-437-05 67877-437 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20160930 N/A ANDA ANDA204453 Ascend Laboratories, LLC MINOCYCLINE HYDROCHLORIDE 80 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-437-05)
67877-437-14 67877-437 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20160930 N/A ANDA ANDA204453 Ascend Laboratories, LLC MINOCYCLINE HYDROCHLORIDE 80 mg/1 10 BLISTER PACK in 1 CARTON (67877-437-14) / 14 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
67877-437-30 67877-437 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20160930 N/A ANDA ANDA204453 Ascend Laboratories, LLC MINOCYCLINE HYDROCHLORIDE 80 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-437-30)
72162-1838-3 72162-1838 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20240311 N/A ANDA ANDA204453 Bryant Ranch Prepack MINOCYCLINE HYDROCHLORIDE 55 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1838-3)
67877-577-01 67877-577 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20160930 N/A ANDA ANDA204453 Ascend Laboratories, LLC MINOCYCLINE HYDROCHLORIDE 135 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-577-01)
67877-577-05 67877-577 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20160930 N/A ANDA ANDA204453 Ascend Laboratories, LLC MINOCYCLINE HYDROCHLORIDE 135 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-577-05)
67877-577-14 67877-577 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20160930 N/A ANDA ANDA204453 Ascend Laboratories, LLC MINOCYCLINE HYDROCHLORIDE 135 mg/1 10 BLISTER PACK in 1 CARTON (67877-577-14) / 14 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
67877-577-30 67877-577 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20160930 N/A ANDA ANDA204453 Ascend Laboratories, LLC MINOCYCLINE HYDROCHLORIDE 135 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-577-30)
67877-436-01 67877-436 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20191223 N/A ANDA ANDA204453 Ascend Laboratories, LLC MINOCYCLINE HYDROCHLORIDE 55 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-436-01)
67877-436-05 67877-436 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20191223 N/A ANDA ANDA204453 Ascend Laboratories, LLC MINOCYCLINE HYDROCHLORIDE 55 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-436-05)
67877-436-14 67877-436 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20191223 N/A ANDA ANDA204453 Ascend Laboratories, LLC MINOCYCLINE HYDROCHLORIDE 55 mg/1 10 BLISTER PACK in 1 CARTON (67877-436-14) / 14 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
67877-436-30 67877-436 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20191223 N/A ANDA ANDA204453 Ascend Laboratories, LLC MINOCYCLINE HYDROCHLORIDE 55 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-436-30)
67877-644-01 67877-644 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20160930 N/A ANDA ANDA204453 Ascend Laboratories, LLC MINOCYCLINE HYDROCHLORIDE 115 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-644-01)
67877-644-05 67877-644 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20160930 N/A ANDA ANDA204453 Ascend Laboratories, LLC MINOCYCLINE HYDROCHLORIDE 115 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-644-05)
67877-644-14 67877-644 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20160930 N/A ANDA ANDA204453 Ascend Laboratories, LLC MINOCYCLINE HYDROCHLORIDE 115 mg/1 10 BLISTER PACK in 1 CARTON (67877-644-14) / 14 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
67877-644-30 67877-644 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20160930 N/A ANDA ANDA204453 Ascend Laboratories, LLC MINOCYCLINE HYDROCHLORIDE 115 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-644-30)
67877-576-01 67877-576 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20160930 N/A ANDA ANDA204453 Ascend Laboratories, LLC MINOCYCLINE HYDROCHLORIDE 90 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-576-01)
67877-438-01 67877-438 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20160930 N/A ANDA ANDA204453 Ascend Laboratories, LLC MINOCYCLINE HYDROCHLORIDE 105 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-438-01)
67877-438-05 67877-438 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20160930 N/A ANDA ANDA204453 Ascend Laboratories, LLC MINOCYCLINE HYDROCHLORIDE 105 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-438-05)
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