Ultra Flex Tablet
Glucosamine sulphate, Chondroitin…
Approved
Registration Information
- Food ID
- 6449
- Status
- Approved
- Application Type
- Generic/Biosimilars
- Classification
- Human
Product Information
- Active Ingredient
- Glucosamine sulphate, Chondroitin…
- Strength
- Glucosamine sulphate 500mg, Chondroitin Sulphate…
- Dosage Form
- Film-Coated Tablet
- Route of Administration
- Oral
- Packaging
- 20's
- Visual Description
- Brilliant blue colored, Oblong, biconvex film…
- Shelf Life
- N/A
Manufacturer Information
- Manufacturer / Site
- KAAP - PHARMACEUTICALS
- MAH (Marketing Authorization Holder)
- ACCRA PHARMACY LTD
- Country
- Pakistan
- Local / Foreign
- Foreign
Record Information
- Last Fetched
- 2026-02-28 02:54:50
- Last Updated
- 2026-10-24 02:54:44
Important Notice
This information is sourced from the Pharmacy and Poisons Board of Kenya. Always consult with a qualified healthcare professional before using any supplement.