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Carvidon-Mr Tablets

NAFDAC Reg. No. B4-4286 · Drug

Registered with NAFDAC. Registration activeAs of 27 October 2026 · synced automatically from official sources.
Product
Carvidon-Mr Tablets
NAFDAC number
B4-4286
Active ingredient
Trimetazidine
Strength
35 mg
Form
Tablet
Pack size
3 x 10's
Manufacturer
Not listed
Applicant (holder)
Micro Nova Pharmaceuticals Ind Ltd
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

  • Carvidon-Mr Tablets is on the NAFDAC register with an active registration (B4-4286). 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 Carvidon-Mr Tablets

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

3 free checks left today Official sources: NAFDAC Green Book & recalls · WHO · U.S. FDA · NLM RxNorm

About Carvidon-Mr Tablets

What is in Carvidon-Mr Tablets?

Carvidon-Mr Tablets contains Trimetazidine (35 mg), as tablet, according to its NAFDAC registration record.

Is Carvidon-Mr Tablets registered with NAFDAC?

Yes. Carvidon-Mr Tablets is listed on the NAFDAC register under registration number B4-4286, and its registration is active as of 27 October 2026.

Has Carvidon-Mr Tablets been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Carvidon-Mr Tablets in our automatically synced alert list.

How can I check that my pack of Carvidon-Mr Tablets is genuine?

Run a free authenticity scan with the NAFDAC number B4-4286, 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.