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Rosart Tablets 50 mg

NAFDAC Reg. No. 04-8238 · Drug

Registered with NAFDAC. Registration activeAs of 28 October 2026 · synced automatically from official sources.
Product
Rosart Tablets 50 mg
NAFDAC number
04-8238
Active ingredient
Losartan Potassium
Strength
50 mg
Form
Tablet
Pack size
5 x 10's (in blisters)
Manufacturer
Not listed
Applicant (holder)
Ranbaxy Nigeria Limited
Approved
26 Apr 2023
Status
Active View on NAFDAC ↗
Registration valid to
25 Apr 2028
WHO alerts
None found
Community reports
None
Times checked
0

What we found

  • Rosart Tablets 50 mg is on the NAFDAC register with an active registration (04-8238). 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 Rosart Tablets 50 mg

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 Rosart Tablets 50 mg

What is in Rosart Tablets 50 mg?

Rosart Tablets 50 mg contains Losartan Potassium (50 mg), as tablet, according to its NAFDAC registration record.

Is Rosart Tablets 50 mg registered with NAFDAC?

Yes. Rosart Tablets 50 mg is listed on the NAFDAC register under registration number 04-8238, and its registration is active as of 28 October 2026.

Has Rosart Tablets 50 mg been flagged as fake or recalled?

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

How can I check that my pack of Rosart Tablets 50 mg is genuine?

Run a free authenticity scan with the NAFDAC number 04-8238, 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.