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 4 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
70771-1158-5 70771-1158 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20250612 N/A ANDA ANDA203553 Zydus Lifesciences Limited MINOCYCLINE HYDROCHLORIDE 115 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1158-5)
70771-1158-7 70771-1158 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20250612 N/A ANDA ANDA203553 Zydus Lifesciences Limited MINOCYCLINE HYDROCHLORIDE 115 mg/1 10 BLISTER PACK in 1 CARTON (70771-1158-7) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
70771-1158-9 70771-1158 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20250612 N/A ANDA ANDA203553 Zydus Lifesciences Limited MINOCYCLINE HYDROCHLORIDE 115 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1158-9)
68382-550-30 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 10 BLISTER PACK in 1 CARTON (68382-550-30) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
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)
70771-1153-0 70771-1153 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20250612 N/A ANDA ANDA203553 Zydus Lifesciences Limited MINOCYCLINE HYDROCHLORIDE 55 mg/1 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1153-0)
70771-1153-1 70771-1153 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20250612 N/A ANDA ANDA203553 Zydus Lifesciences Limited MINOCYCLINE HYDROCHLORIDE 55 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1153-1)
70771-1153-3 70771-1153 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20250612 N/A ANDA ANDA203553 Zydus Lifesciences Limited MINOCYCLINE HYDROCHLORIDE 55 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1153-3)
70771-1153-5 70771-1153 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20250612 N/A ANDA ANDA203553 Zydus Lifesciences Limited MINOCYCLINE HYDROCHLORIDE 55 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1153-5)
70771-1153-7 70771-1153 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20250612 N/A ANDA ANDA203553 Zydus Lifesciences Limited MINOCYCLINE HYDROCHLORIDE 55 mg/1 10 BLISTER PACK in 1 CARTON (70771-1153-7) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
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)
70771-1155-0 70771-1155 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20180307 N/A ANDA ANDA203553 Zydus Lifesciences Limited MINOCYCLINE HYDROCHLORIDE 80 mg/1 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1155-0)
70771-1155-1 70771-1155 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20180307 N/A ANDA ANDA203553 Zydus Lifesciences Limited MINOCYCLINE HYDROCHLORIDE 80 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1155-1)
70771-1155-3 70771-1155 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20180307 N/A ANDA ANDA203553 Zydus Lifesciences Limited MINOCYCLINE HYDROCHLORIDE 80 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1155-3)
70771-1155-5 70771-1155 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20180307 N/A ANDA ANDA203553 Zydus Lifesciences Limited MINOCYCLINE HYDROCHLORIDE 80 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1155-5)
70771-1155-7 70771-1155 HUMAN PRESCRIPTION DRUG minocycline hydrochloride minocycline hydrochloride TABLET, EXTENDED RELEASE ORAL 20180307 N/A ANDA ANDA203553 Zydus Lifesciences Limited MINOCYCLINE HYDROCHLORIDE 80 mg/1 10 BLISTER PACK in 1 CARTON (70771-1155-7) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
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