- Approval Id
- c4e94b61bd657087
- Drug Name
- FEXOFEN FILM-COATED TABLET 180MG
- Product Name
- FEXOFEN FILM-COATED TABLET 180MG
- Approval Number
- SIN16296P
- Approval Date
- 2021-08-10
- Registrant
- GOLDPLUS UNIVERSAL PTE LTD
- Licence Holder
- GOLDPLUS UNIVERSAL PTE LTD
- Drug Type
- Therapeutic
- Forensic Classification
- Prescription Only
- Dosage Form
- TABLET, FILM COATED
- Dosage
- <p><strong>DOSAGE & METHOD OF ADMINISTRATION:</strong><br>
<strong>Adults and children aged 12 years and older</strong><br>
The recommended dose is one tablet once daily.<br>
<strong>Special risk groups</strong><br>
Studies in special risk groups (elderly, renally or hepatically impaired patients) indicate that it is not necessary to adjust the dose of fexofenadine hydrochloride in these patients.</p>
- Route Of Administration
- ORAL
- Indication Info
- <p><strong>INDICATIONS & USAGE:</strong><br>
Fexofenadine Hydrochloride Tablets USP is indicated in adults and children 12 years and older for followings:</p>
<ul class="dash">
<li>Relief of symptoms associated with seasonal allergic rhinitis.</li>
<li>Relief of symptoms associated with chronic idiopathic urticaria.</li>
</ul>
- Contraindications
- <p><strong>CONTRAINDICATION:</strong><br>
Hypersensitivity to the active substance or to any of the excipients listed.</p>
- Atc Code
- R06AX26
- Atc Item Name
- fexofenadine
- Pharma Manufacturer Name
- GOLDPLUS UNIVERSAL PTE LTD
