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Home / Drug A–Z / Czartan 25 Tablets

Czartan 25 Tablets

NAFDAC Reg. No. B4-3978 · Drug

Registered with NAFDAC. Registration activeAs of 28 October 2026 · synced automatically from official sources.
Product
Czartan 25 Tablets
NAFDAC number
B4-3978
Active ingredient
Losartan Potassium
Strength
25 mg
Form
Tablet
Manufacturer
Not listed
Applicant (holder)
JMD Pharmalinks Limited
Approved
2 Dec 2021
Status
Active View on NAFDAC ↗
Registration valid to
1 Dec 2026
WHO alerts
None found
Community reports
None
Times checked
0

What we found

  • Czartan 25 Tablets is on the NAFDAC register with an active registration (B4-3978). 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 Czartan 25 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 Czartan 25 Tablets

What is in Czartan 25 Tablets?

Czartan 25 Tablets contains Losartan Potassium (25 mg), as tablet, according to its NAFDAC registration record.

Is Czartan 25 Tablets registered with NAFDAC?

Yes. Czartan 25 Tablets is listed on the NAFDAC register under registration number B4-3978, and its registration is active as of 28 October 2026.

Has Czartan 25 Tablets been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Czartan 25 Tablets in our automatically synced alert list.

How can I check that my pack of Czartan 25 Tablets is genuine?

Run a free authenticity scan with the NAFDAC number B4-3978, 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.