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=ANDA211023"
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
60687-417-71 60687-417 HUMAN PRESCRIPTION DRUG Hydrocodone Bitartrate and Acetaminophen Hydrocodone Bitartrate and Acetaminophen SOLUTION ORAL 20190619 N/A ANDA ANDA211023 American Health Packaging ACETAMINOPHEN; HYDROCODONE BITARTRATE 325 mg/15mL; 7.5 mg/15mL 5 TRAY in 1 CASE (60687-417-71) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-417-50) / 15 mL in 1 CUP, UNIT-DOSE (60687-417-44)
71930-027-43 71930-027 HUMAN PRESCRIPTION DRUG Hydrocodone Bitartrate and Acetaminophen Hydrocodone Bitartrate and Acetaminophen SOLUTION ORAL 20190408 N/A ANDA ANDA211023 Eywa Pharma Inc ACETAMINOPHEN; HYDROCODONE BITARTRATE 325 mg/15mL; 7.5 mg/15mL 473 mL in 1 BOTTLE (71930-027-43)
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