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"
符合检索条件的记录共 60 条，共 3 页，当前第 2 页 ，可点击列名称排序
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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
72162-1840-3 72162-1840 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20230421 N/A ANDA ANDA204453 Bryant Ranch Prepack MINOCYCLINE HYDROCHLORIDE 105 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1840-3)
67877-643-14 67877-643 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20160930 N/A ANDA ANDA204453 Ascend Laboratories, LLC MINOCYCLINE HYDROCHLORIDE 65 mg/1 10 BLISTER PACK in 1 CARTON (67877-643-14) / 14 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
67877-643-30 67877-643 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20160930 N/A ANDA ANDA204453 Ascend Laboratories, LLC MINOCYCLINE HYDROCHLORIDE 65 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-643-30)
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)
72162-1867-3 72162-1867 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20240311 N/A ANDA ANDA204453 Bryant Ranch Prepack MINOCYCLINE HYDROCHLORIDE 65 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1867-3)
72162-1868-3 72162-1868 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20240311 N/A ANDA ANDA204453 Bryant Ranch Prepack MINOCYCLINE HYDROCHLORIDE 115 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1868-3)
72162-1852-3 72162-1852 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20240311 N/A ANDA ANDA204453 Bryant Ranch Prepack MINOCYCLINE HYDROCHLORIDE 90 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1852-3)
72162-1853-3 72162-1853 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20240311 N/A ANDA ANDA204453 Bryant Ranch Prepack MINOCYCLINE HYDROCHLORIDE 135 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1853-3)
72162-1854-3 72162-1854 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20240311 N/A ANDA ANDA204453 Bryant Ranch Prepack MINOCYCLINE HYDROCHLORIDE 45 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1854-3)
72789-523-30 72789-523 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20250910 N/A ANDA ANDA204453 PD-Rx Pharmaceuticals, Inc. MINOCYCLINE HYDROCHLORIDE 45 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-523-30)
72789-527-30 72789-527 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20250910 N/A ANDA ANDA204453 PD-Rx Pharmaceuticals, Inc. MINOCYCLINE HYDROCHLORIDE 80 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-527-30)
72789-528-30 72789-528 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20250910 N/A ANDA ANDA204453 PD-Rx Pharmaceuticals, Inc. MINOCYCLINE HYDROCHLORIDE 105 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-528-30)
72789-529-30 72789-529 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20250910 N/A ANDA ANDA204453 PD-Rx Pharmaceuticals, Inc. MINOCYCLINE HYDROCHLORIDE 115 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-529-30)
72789-530-30 72789-530 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20250910 N/A ANDA ANDA204453 PD-Rx Pharmaceuticals, Inc. MINOCYCLINE HYDROCHLORIDE 135 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-530-30)
71335-2710-1 71335-2710 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20250728 N/A ANDA ANDA204453 Bryant Ranch Prepack MINOCYCLINE HYDROCHLORIDE 90 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2710-1)
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)
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