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=ANDA218157"
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
70756-312-30 70756-312 HUMAN PRESCRIPTION DRUG Telmisartan Telmisartan TABLET ORAL 20241015 N/A ANDA ANDA218157 Lifestar Pharma LLC TELMISARTAN 20 mg/1 30 TABLET in 1 BOTTLE (70756-312-30)
70756-312-99 70756-312 HUMAN PRESCRIPTION DRUG Telmisartan Telmisartan TABLET ORAL 20241015 N/A ANDA ANDA218157 Lifestar Pharma LLC TELMISARTAN 20 mg/1 10 BLISTER PACK in 1 CARTON (70756-312-99) / 10 TABLET in 1 BLISTER PACK (70756-312-01)
70756-313-30 70756-313 HUMAN PRESCRIPTION DRUG Telmisartan Telmisartan TABLET ORAL 20241015 N/A ANDA ANDA218157 Lifestar Pharma LLC TELMISARTAN 40 mg/1 30 TABLET in 1 BOTTLE (70756-313-30)
70756-313-80 70756-313 HUMAN PRESCRIPTION DRUG Telmisartan Telmisartan TABLET ORAL 20241015 N/A ANDA ANDA218157 Lifestar Pharma LLC TELMISARTAN 40 mg/1 8 BLISTER PACK in 1 CARTON (70756-313-80) / 10 TABLET in 1 BLISTER PACK (70756-313-01)
70756-314-30 70756-314 HUMAN PRESCRIPTION DRUG Telmisartan Telmisartan TABLET ORAL 20241015 N/A ANDA ANDA218157 Lifestar Pharma LLC TELMISARTAN 80 mg/1 30 TABLET in 1 BOTTLE (70756-314-30)
70756-314-80 70756-314 HUMAN PRESCRIPTION DRUG Telmisartan Telmisartan TABLET ORAL 20241015 N/A ANDA ANDA218157 Lifestar Pharma LLC TELMISARTAN 80 mg/1 8 BLISTER PACK in 1 CARTON (70756-314-80) / 10 TABLET in 1 BLISTER PACK (70756-314-01)
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