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Gliptus 50 mg Tablets_

NAFDAC Reg. No. B4-9402 · Drug

Registered with NAFDAC. Registration activeAs of 28 October 2026 · synced automatically from official sources.
Product
Gliptus 50 mg Tablets_
NAFDAC number
B4-9402
Active ingredient
Vildagliptin
Strength
50 mg
Form
Tablet
Pack size
3 x 10's (in Alu-Alu blisters)
Manufacturer
Not listed
Applicant (holder)
EVA SCIENCES NIGERIA LIMITED
Approved
27 Aug 2025
Status
Active View on NAFDAC ↗
Registration valid to
26 Aug 2030
WHO alerts
None found
Community reports
None
Times checked
0

What we found

  • Gliptus 50 mg Tablets_ is on the NAFDAC register with an active registration (B4-9402). 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.

How to use Gliptus 50 mg Tablets_

What the official label says. If a doctor prescribed it, follow the prescription. Your pack's leaflet comes first if it is different.

Who it is for

relieves: • heartburn • sour stomach • acid indigestion • upset stomach associated with these symptoms

How to take it and how often
  • Adults and
  • Children 12 years of age and over: chew 2-4 tablets as symptoms occur, or as directed by a doctor
  • Do not
  • Swallow tablets whole. • do not take for symptoms that persist for more than 2 weeks unless advised by a doctor
Warnings

Ask a doctor or pharmacist before use if you are taking a prescription drug. Antacids may interact with certain prescription drugs. When using this product • do not take more than 15 tablets in 24 hours • do not use the maximum dosage for more than 2 weeks except under the advice and supervision of a doctor

If you miss a dose

Take it when you remember, unless it is nearly time for the next dose. Then skip the missed one. Never take two doses at once to make up for it. Check your leaflet, as some medicines are different.

From the official U.S. FDA label for this active ingredient. Your pack may have a different strength, so always read its leaflet. If a doctor prescribed it, follow the prescription. Ask a pharmacist if you are unsure. Label dated 2024-10-25.

Label for Gliptus 50 mg Tablets_, the active ingredient registered with NAFDAC.

Check your pack of Gliptus 50 mg Tablets_

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 Gliptus 50 mg Tablets_

What is in Gliptus 50 mg Tablets_?

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

Is Gliptus 50 mg Tablets_ registered with NAFDAC?

Yes. Gliptus 50 mg Tablets_ is listed on the NAFDAC register under registration number B4-9402, and its registration is active as of 28 October 2026.

Has Gliptus 50 mg Tablets_ been flagged as fake or recalled?

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

How can I check that my pack of Gliptus 50 mg Tablets_ is genuine?

Run a free authenticity scan with the NAFDAC number B4-9402, 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.

How do I take Gliptus 50 mg Tablets_?

Follow your prescription or the leaflet in your pack. The official label says: • adults and children 12 years of age and over: chew 2-4 tablets as symptoms occur, or as directed by a doctor. Do not swallow tablets whole. • do not take for symptoms that persist for more than 2 weeks unless advised by a doctor…

What is Gliptus 50 mg Tablets_ used for?

relieves: • heartburn • sour stomach • acid indigestion • upset stomach associated with these symptoms (Summarised from the official U.S. FDA label for Gliptus 50 mg Tablets_. Always follow your doctor or pharmacist.)

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