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Vilget 50 mg Tablet

NAFDAC Reg. No. B4-9698 · Drug

Registered with NAFDAC. Registration activeAs of 28 October 2026 · synced automatically from official sources.
Product
Vilget 50 mg Tablet
NAFDAC number
B4-9698
Active ingredient
Vildagliptin
Strength
50 mg
Form
Tablet
Pack size
3 x 10's (in Alu-Alu blisters)
Manufacturer
Not listed
Applicant (holder)
Getz Pharma Nigeria Limited
Approved
21 Dec 2023
Status
Active View on NAFDAC ↗
Registration valid to
20 Dec 2028
WHO alerts
None found
Community reports
None
Times checked
0

What we found

  • Vilget 50 mg Tablet is on the NAFDAC register with an active registration (B4-9698). A valid number alone does not prove a pack is genuine — counterfeiters copy real numbers, so also check the expiry date, seal and print quality.

Generated automatically from the NAFDAC register, WHO alerts and community data as of today. This is not medical advice. Always follow your doctor or pharmacist.

Check your pack of Vilget 50 mg Tablet

Add the expiry date on your pack for a full Trust Score.

3 free checks left today Official sources: NAFDAC · WHO · U.S. FDA · Health Canada · NLM

About Vilget 50 mg Tablet

What is in Vilget 50 mg Tablet?

Vilget 50 mg Tablet contains Vildagliptin (50 mg), as tablet, according to its NAFDAC registration record.

Is Vilget 50 mg Tablet registered with NAFDAC?

Yes. Vilget 50 mg Tablet is listed on the NAFDAC register under registration number B4-9698, and its registration is active as of 28 October 2026.

Has Vilget 50 mg Tablet been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Vilget 50 mg Tablet in our automatically synced alert list.

How can I check that my pack of Vilget 50 mg Tablet is genuine?

Run a free authenticity scan with the NAFDAC number B4-9698, your pack's expiry date and batch number to get a Trust Score, compare the pack with the NAFDAC record (ingredient, strength, form, manufacturer), and buy only from licensed pharmacies.

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Reviews are personal experiences from PillVera users, not medical advice. Report side effects to your doctor and to NAFDAC.