Kenzotakara
N/A
Approved
Registration Information
- Food ID
- 4639
- Status
- Approved
- Application Type
- Generic/Biosimilars
- Classification
- Human
Product Information
- Active Ingredient
- N/A
- Strength
- 100g
- Dosage Form
- Powder And Solvent For Sealant
- Route of Administration
- Conjunctival
- Packaging
- Small Box x 12 sachets
- Visual Description
- Sachets
- Shelf Life
- N/A
Manufacturer Information
- Manufacturer / Site
- DYNAPHARM (M) SDN BHD
- MAH (Marketing Authorization Holder)
- DYNAPHARM (M) SDN BHD
- Country
- Finland
- Local / Foreign
- Foreign
Record Information
- Last Fetched
- 2026-02-28 02:38:32
- Last Updated
- 2026-09-23 02:38:37
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.