Recorded Chinese product: 克霉唑阴道泡腾片克霉唑阴道泡腾片
This is a medicine registration record from NMPA data.本页为国家药监局药品注册记录。
Labeled sections from the recorded Chinese source are included below. English wording is a reference translation when one is on file, not an official English label.本记录未接入产品级适应症/安全性标注字段。
生产企业Manufacturer
- 哈尔滨凯程制药有限公司Chinese legal name: 哈尔滨凯程制药有限公司
主要成分Active Ingredients
- 克霉唑BKemei Zuo
药物知识说明
克霉唑B是一种在国家药监局注册认定的药品。该药品含有克霉唑b-4dcaa4b8等成分。
该药品关联的活性成分包括:克霉唑b。这些成分信息来自国家药监局数据库。
该药品标注的生产企业为:哈尔滨凯程制药有限公司Chinese legal name: 哈尔滨凯程制药有限公司。
您可以探索含有相同成分的其他药品:克霉唑b-4dcaa4b8成分药品。
本页面内容来自国家药监局数据库,MedicineGraph在此基础上提供关系图谱和知识导航。
Medicine Knowledge
This medicine (original name: 克霉唑阴道泡腾片) is a medicine registered with the national drug regulatory authority. It contains recorded ingredients as active ingredient(s).
Manufacturers recorded for this product: 哈尔滨凯程制药有限公司Chinese legal name: 哈尔滨凯程制药有限公司.
Explore other medicines containing the same ingredient: 克霉唑b productsProducts containing this recorded ingredient.
Source: MedicineGraph authoritative database. Relationships derived from registered product information.
这是什么What is this
- 通用名/品名Recorded product name: 克霉唑阴道泡腾片Recorded Chinese product: 克霉唑阴道泡腾片
- 剂型Dosage form: 片剂Tablets
- 规格Specification: 0.15g。0.15 g
本段仅展示注册/说明书已记录的身份属性,不含适应症或用法建议。Identity attributes from registration/leaflet records only; no indications or usage advice.
生产企业Manufacturer
- 哈尔滨凯程制药有限公司Chinese legal name: 哈尔滨凯程制药有限公司
注册信息NMPA approval number
- 批准文号NMPA approval number: 国药准字H20074190
关联实体Relationships
信息来源Source and scope
国家药品监督管理局(中国)药品注册数据及已接入说明书字段。National Medical Products Administration (China) medicine-registration data and linked leaflet fields.
- 品名来源Name source: 10多万条药品说明书数据库 (HIGH)Package-insert database (more than 100,000 records) (HIGH)
- 生产企业来源Manufacturer source: 10多万条药品说明书数据库Package-insert database (more than 100,000 records)
- 剂型来源Dosage-form source: 10多万条药品说明书数据库Package-insert database (more than 100,000 records)
范围:当前 MedicineGraph 注册记录及已记录的精确关系;非完整目录,亦不构成疗效等同主张,也不支持换用判断。不含适应症/安全性推断。Scope: current MedicineGraph registration records and exact recorded relationships; not a complete catalog and not a claim of therapeutic equivalence. No inferred indications/safety.
本段为已核准说明书原文摘录(非改写、非AI摘要),非正式英文标签,亦不构成用药建议。 Not an official English label and not medical advice. English wording, when shown, is a reference translation of the Chinese source label.
English translation for reference. Translated from the Chinese source label. Not an official English label and not medical advice.
NMPA approval number
国药准字H20074190
Manufacturer
Chinese legal name: 哈尔滨凯程制药有限公司 (domestically manufactured)
Indications
English translation unavailable. The original Chinese source label remains available below.
Dosage and administration
English translation unavailable. The original Chinese source label remains available below.
Adverse reactions
English translation unavailable. The original Chinese source label remains available below.
Contraindications
English translation unavailable. The original Chinese source label remains available below.
Precautions
English translation unavailable. The original Chinese source label remains available below.
Storage
English translation unavailable. The original Chinese source label remains available below.
Specification
English translation unavailable. The original Chinese source label remains available below.
中文说明书原文Original Chinese source label
批准文号
国药准字H20074190
生产企业
哈尔滨凯程制药有限公司(国产)
适应症
用于念珠菌性外阴阴道病。
用法用量
阴道给药。每晚睡前1片,塞入阴道深处。10日为一疗程。
不良反应
偶见局部刺激,如瘙痒或烧灼感。个别患者使用本品后可能出现不同程度的过敏等不良反应,包括红斑、呼吸短促、低血压或短暂的感觉减损、恶心、腹泻等。
禁忌
对本品过敏者禁用。
注意事项
1.本品仅供阴道给药,切忌口服。2.孕妇应尽量避免使用,并应在医师指导下使用。3.哺乳期妇女慎用。4.无性生活史的女性应在医师指导下使用。5.使用本品时应避开月经期。6.用药部位如有烧灼感、红肿等情况应停药,并将局部药物洗净,必要时向医师咨询。7.用药期间注意个人卫生,防止重复感染,使用避孕套或避免房事。8.给药时应洗净双手或戴指套或手套。9.对本品过敏者禁用,过敏体质者慎用。10.本品性状发生改变时禁止使用。11.请将本品放在儿童不能接触的地方。12.如正在使用其他药品,使用本品前请咨询医师或药师。
贮藏
密封
规格
0.15g。
信息来源Source and scope
国家药品监督管理局(中国)药品注册数据。National Medical Products Administration (China) medicine-registration data.
范围:当前 MedicineGraph 注册记录及已记录的精确关系;非完整目录,亦不构成疗效等同主张,也不支持换用判断。Scope: current MedicineGraph registration records and exact recorded relationships; not a complete catalog and not a claim of therapeutic equivalence.