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=ANDA208605"
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
72241-015-10 72241-015 HUMAN PRESCRIPTION DRUG Telmisartan Telmisartan TABLET ORAL 20221222 N/A ANDA ANDA208605 Modavar Pharmaceuticals LLC TELMISARTAN 20 mg/1 500 TABLET in 1 BOTTLE (72241-015-10)
72241-015-11 72241-015 HUMAN PRESCRIPTION DRUG Telmisartan Telmisartan TABLET ORAL 20221222 N/A ANDA ANDA208605 Modavar Pharmaceuticals LLC TELMISARTAN 20 mg/1 1000 TABLET in 1 BOTTLE (72241-015-11)
72241-015-16 72241-015 HUMAN PRESCRIPTION DRUG Telmisartan Telmisartan TABLET ORAL 20150205 N/A ANDA ANDA208605 Modavar Pharmaceuticals LLC TELMISARTAN 20 mg/1 30 BLISTER PACK in 1 CARTON (72241-015-16) / 10 TABLET in 1 BLISTER PACK
72241-015-18 72241-015 HUMAN PRESCRIPTION DRUG Telmisartan Telmisartan TABLET ORAL 20150205 N/A ANDA ANDA208605 Modavar Pharmaceuticals LLC TELMISARTAN 20 mg/1 30 BLISTER PACK in 1 CARTON (72241-015-18) / 10 TABLET in 1 BLISTER PACK
72241-015-22 72241-015 HUMAN PRESCRIPTION DRUG Telmisartan Telmisartan TABLET ORAL 20221222 N/A ANDA ANDA208605 Modavar Pharmaceuticals LLC TELMISARTAN 20 mg/1 30 TABLET in 1 BOTTLE (72241-015-22)
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