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=ANDA203553"
符合检索条件的记录共 96 条，共 5 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
68382-533-05 68382-533 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20180307 N/A ANDA ANDA203553 Zydus Pharmaceuticals (USA) Inc. MINOCYCLINE HYDROCHLORIDE 90 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-533-05)
68382-533-06 68382-533 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20180307 N/A ANDA ANDA203553 Zydus Pharmaceuticals (USA) Inc. MINOCYCLINE HYDROCHLORIDE 90 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-533-06)
68382-533-10 68382-533 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20180307 N/A ANDA ANDA203553 Zydus Pharmaceuticals (USA) Inc. MINOCYCLINE HYDROCHLORIDE 90 mg/1 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-533-10)
68382-533-16 68382-533 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20180307 N/A ANDA ANDA203553 Zydus Pharmaceuticals (USA) Inc. MINOCYCLINE HYDROCHLORIDE 90 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-533-16)
68382-533-30 68382-533 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20180307 N/A ANDA ANDA203553 Zydus Pharmaceuticals (USA) Inc. MINOCYCLINE HYDROCHLORIDE 90 mg/1 10 BLISTER PACK in 1 CARTON (68382-533-30) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
68382-551-01 68382-551 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20180307 N/A ANDA ANDA203553 Zydus Pharmaceuticals (USA) Inc. MINOCYCLINE HYDROCHLORIDE 80 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-551-01)
68382-551-05 68382-551 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20180307 N/A ANDA ANDA203553 Zydus Pharmaceuticals (USA) Inc. MINOCYCLINE HYDROCHLORIDE 80 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-551-05)
68382-551-06 68382-551 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20180307 N/A ANDA ANDA203553 Zydus Pharmaceuticals (USA) Inc. MINOCYCLINE HYDROCHLORIDE 80 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-551-06)
68382-551-10 68382-551 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20180307 N/A ANDA ANDA203553 Zydus Pharmaceuticals (USA) Inc. MINOCYCLINE HYDROCHLORIDE 80 mg/1 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-551-10)
68382-551-16 68382-551 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20180307 N/A ANDA ANDA203553 Zydus Pharmaceuticals (USA) Inc. MINOCYCLINE HYDROCHLORIDE 80 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-551-16)
68382-551-30 68382-551 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20180307 N/A ANDA ANDA203553 Zydus Pharmaceuticals (USA) Inc. MINOCYCLINE HYDROCHLORIDE 80 mg/1 10 BLISTER PACK in 1 CARTON (68382-551-30) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
70771-1157-9 70771-1157 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20180307 N/A ANDA ANDA203553 Zydus Lifesciences Limited MINOCYCLINE HYDROCHLORIDE 105 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1157-9)
68382-550-06 68382-550 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20250612 N/A ANDA ANDA203553 Zydus Pharmaceuticals (USA) Inc. MINOCYCLINE HYDROCHLORIDE 55 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-550-06)
68382-550-10 68382-550 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20250612 N/A ANDA ANDA203553 Zydus Pharmaceuticals (USA) Inc. MINOCYCLINE HYDROCHLORIDE 55 mg/1 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-550-10)
68382-550-16 68382-550 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20250612 N/A ANDA ANDA203553 Zydus Pharmaceuticals (USA) Inc. MINOCYCLINE HYDROCHLORIDE 55 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-550-16)
68382-532-01 68382-532 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20250612 N/A ANDA ANDA203553 Zydus Pharmaceuticals (USA) Inc. MINOCYCLINE HYDROCHLORIDE 65 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-532-01)
68382-532-05 68382-532 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20250612 N/A ANDA ANDA203553 Zydus Pharmaceuticals (USA) Inc. MINOCYCLINE HYDROCHLORIDE 65 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-532-05)
68382-532-06 68382-532 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20250612 N/A ANDA ANDA203553 Zydus Pharmaceuticals (USA) Inc. MINOCYCLINE HYDROCHLORIDE 65 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-532-06)
68382-532-10 68382-532 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20250612 N/A ANDA ANDA203553 Zydus Pharmaceuticals (USA) Inc. MINOCYCLINE HYDROCHLORIDE 65 mg/1 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-532-10)
68382-532-16 68382-532 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20250612 N/A ANDA ANDA203553 Zydus Pharmaceuticals (USA) Inc. MINOCYCLINE HYDROCHLORIDE 65 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-532-16)
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