ArthroXtra™ Tablets*
N/A
Approved
Registration Information
- Food ID
- 1954
- Status
- Approved
- Application Type
- New/Innovator
- Classification
- Human
Product Information
- Active Ingredient
- N/A
- Strength
- Each tablet contains: Glucosamine Hydrochloride…
- Dosage Form
- Coated Tablet
- Route of Administration
- Oral
- Packaging
- 60 tablets/bottle; HDPE
- Visual Description
- White, film coated, capsule-shaped tablet with…
- Shelf Life
- N/A
Manufacturer Information
- Manufacturer / Site
- "BF Suma Pharmaceuticals Inc. Address: 5077…
- MAH (Marketing Authorization Holder)
- "Lok Wah Development Limited Akara bldg, 24 De…
- Country
- United States
- Local / Foreign
- Foreign
Record Information
- Last Fetched
- 2026-02-28 02:17:08
- Last Updated
- 2026-09-23 02:17:08
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.