MAGNILAX
N/A
Approved
Registration Information
- Food ID
- 13404
- Status
- Approved
- Application Type
- New/Innovator
- Classification
- Human
Product Information
- Active Ingredient
- N/A
- Strength
- 400MG
- Dosage Form
- Tablet
- Route of Administration
- Oral
- Packaging
- 30 tablets per serving
- Visual Description
- Yellow oblong, biconvex plain coated on both sides
- Shelf Life
- N/A
Manufacturer Information
- Manufacturer / Site
- Nutrifactor Laboratories (Pvt) Ltd.
- MAH (Marketing Authorization Holder)
- Nutrifactor Laboratories(Pvt.) Limited
- Country
- Pakistan
- Local / Foreign
- Foreign
Record Information
- Last Fetched
- 2026-02-28 03:54:11
- Last Updated
- 2026-11-11 03:55:31
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.