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
67877-436-01 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)
67877-437-01 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)
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)
67877-438-14 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 10 BLISTER PACK in 1 CARTON (67877-438-14) / 14 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
67877-438-30 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 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-438-30)
63629-9208-1 63629-9208 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20220302 N/A ANDA ANDA204453 Bryant Ranch Prepack MINOCYCLINE HYDROCHLORIDE 105 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9208-1)
63629-9209-1 63629-9209 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20220302 N/A ANDA ANDA204453 Bryant Ranch Prepack MINOCYCLINE HYDROCHLORIDE 115 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9209-1)
63629-9210-1 63629-9210 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20220302 N/A ANDA ANDA204453 Bryant Ranch Prepack MINOCYCLINE HYDROCHLORIDE 135 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9210-1)
63629-9211-1 63629-9211 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20220302 N/A ANDA ANDA204453 Bryant Ranch Prepack MINOCYCLINE HYDROCHLORIDE 45 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9211-1)
63629-9212-1 63629-9212 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20220302 N/A ANDA ANDA204453 Bryant Ranch Prepack MINOCYCLINE HYDROCHLORIDE 55 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9212-1)
63629-9213-1 63629-9213 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20220302 N/A ANDA ANDA204453 Bryant Ranch Prepack MINOCYCLINE HYDROCHLORIDE 65 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9213-1)
63629-9214-1 63629-9214 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20220302 N/A ANDA ANDA204453 Bryant Ranch Prepack MINOCYCLINE HYDROCHLORIDE 80 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9214-1)
63629-9215-1 63629-9215 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20220302 N/A ANDA ANDA204453 Bryant Ranch Prepack MINOCYCLINE HYDROCHLORIDE 90 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9215-1)
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