OSTEONIX
N/A
Approved
Registration Information
- Food ID
- 14865
- Status
- Approved
- Application Type
- Generic/Biosimilars
- Classification
- Human
Product Information
- Active Ingredient
- N/A
- Strength
- Chondroitin Sulphate Sodium USP 200 mg…
- Dosage Form
- Tablet
- Route of Administration
- Oral
- Packaging
- 3X1x10 Tablets in carton with pack insert
- Visual Description
- Brown coloured, capsule shaped film coated tablet.
- Shelf Life
- N/A
Manufacturer Information
- Manufacturer / Site
- INNOVATIVE HEALTHCARE
- MAH (Marketing Authorization Holder)
- DUA HEALTHCARE LIMITED
- Country
- India
- Local / Foreign
- Foreign
Record Information
- Last Fetched
- 2026-02-28 04:06:27
- Last Updated
- 2026-09-23 04:06:25
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.