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
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)
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)
72789-524-30 72789-524 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20250910 N/A ANDA ANDA204453 PD-Rx Pharmaceuticals, Inc. MINOCYCLINE HYDROCHLORIDE 65 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-524-30)
72789-525-30 72789-525 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20250910 N/A ANDA ANDA204453 PD-Rx Pharmaceuticals, Inc. MINOCYCLINE HYDROCHLORIDE 90 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-525-30)
72789-526-30 72789-526 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20250910 N/A ANDA ANDA204453 PD-Rx Pharmaceuticals, Inc. MINOCYCLINE HYDROCHLORIDE 55 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-526-30)
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)
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)
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)
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)
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)
71335-2711-1 71335-2711 HUMAN PRESCRIPTION DRUG Minocycline Hydrochloride Minocycline Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20250728 N/A ANDA ANDA204453 Bryant Ranch Prepack MINOCYCLINE HYDROCHLORIDE 45 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2711-1)
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)
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)
63629-9213-1 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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