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=ANDA040616"
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
0093-1716-01 0093-1716 HUMAN PRESCRIPTION DRUG Warfarin Sodium Warfarin Sodium TABLET ORAL 20150609 N/A ANDA ANDA040616 Teva Pharmaceuticals USA, Inc. WARFARIN SODIUM 4 mg/1 100 TABLET in 1 BOTTLE (0093-1716-01)
0093-1716-10 0093-1716 HUMAN PRESCRIPTION DRUG Warfarin Sodium Warfarin Sodium TABLET ORAL 20150818 N/A ANDA ANDA040616 Teva Pharmaceuticals USA, Inc. WARFARIN SODIUM 4 mg/1 1000 TABLET in 1 BOTTLE (0093-1716-10)
70518-0253-0 70518-0253 HUMAN PRESCRIPTION DRUG Warfarin Sodium Warfarin Sodium TABLET ORAL 20170223 N/A ANDA ANDA040616 REMEDYREPACK INC. WARFARIN SODIUM 5 mg/1 30 TABLET in 1 BLISTER PACK (70518-0253-0)
70518-0273-0 70518-0273 HUMAN PRESCRIPTION DRUG Warfarin Sodium Warfarin Sodium TABLET ORAL 20170302 N/A ANDA ANDA040616 REMEDYREPACK INC. WARFARIN SODIUM 3 mg/1 30 TABLET in 1 BLISTER PACK (70518-0273-0)
0093-1723-01 0093-1723 HUMAN PRESCRIPTION DRUG Warfarin Sodium Warfarin Sodium TABLET ORAL 20180827 N/A ANDA ANDA040616 Teva Pharmaceuticals USA, Inc. WARFARIN SODIUM 7.5 mg/1 100 TABLET in 1 BOTTLE (0093-1723-01)
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