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 60 条，共 3 页，当前第 3 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
68382-531-16 68382-531 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20180307 N/A ANDA ANDA203553 Zydus Pharmaceuticals (USA) Inc. MINOCYCLINE HYDROCHLORIDE 45 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-531-16)
68382-531-30 68382-531 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20180307 N/A ANDA ANDA203553 Zydus Pharmaceuticals (USA) Inc. MINOCYCLINE HYDROCHLORIDE 45 mg/1 10 BLISTER PACK in 1 CARTON (68382-531-30) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
70771-1156-7 70771-1156 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20180307 N/A ANDA ANDA203553 Zydus Lifesciences Limited MINOCYCLINE HYDROCHLORIDE 90 mg/1 10 BLISTER PACK in 1 CARTON (70771-1156-7) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
70771-1156-9 70771-1156 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20180307 N/A ANDA ANDA203553 Zydus Lifesciences Limited MINOCYCLINE HYDROCHLORIDE 90 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1156-9)
70771-1156-0 70771-1156 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20180307 N/A ANDA ANDA203553 Zydus Lifesciences Limited MINOCYCLINE HYDROCHLORIDE 90 mg/1 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1156-0)
70771-1156-1 70771-1156 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20180307 N/A ANDA ANDA203553 Zydus Lifesciences Limited MINOCYCLINE HYDROCHLORIDE 90 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1156-1)
70771-1156-3 70771-1156 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20180307 N/A ANDA ANDA203553 Zydus Lifesciences Limited MINOCYCLINE HYDROCHLORIDE 90 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1156-3)
70771-1156-5 70771-1156 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20180307 N/A ANDA ANDA203553 Zydus Lifesciences Limited MINOCYCLINE HYDROCHLORIDE 90 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1156-5)
68382-535-01 68382-535 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20180307 N/A ANDA ANDA203553 Zydus Pharmaceuticals (USA) Inc. MINOCYCLINE HYDROCHLORIDE 135 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-535-01)
68382-535-05 68382-535 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20180307 N/A ANDA ANDA203553 Zydus Pharmaceuticals (USA) Inc. MINOCYCLINE HYDROCHLORIDE 135 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-535-05)
68382-535-06 68382-535 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20180307 N/A ANDA ANDA203553 Zydus Pharmaceuticals (USA) Inc. MINOCYCLINE HYDROCHLORIDE 135 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-535-06)
68382-535-10 68382-535 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20180307 N/A ANDA ANDA203553 Zydus Pharmaceuticals (USA) Inc. MINOCYCLINE HYDROCHLORIDE 135 mg/1 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-535-10)
68382-535-16 68382-535 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20180307 N/A ANDA ANDA203553 Zydus Pharmaceuticals (USA) Inc. MINOCYCLINE HYDROCHLORIDE 135 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-535-16)
68382-535-30 68382-535 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20180307 N/A ANDA ANDA203553 Zydus Pharmaceuticals (USA) Inc. MINOCYCLINE HYDROCHLORIDE 135 mg/1 10 BLISTER PACK in 1 CARTON (68382-535-30) / 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
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