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Sukkar Blood Glucose Monitoring Device

NAFDAC Reg. No. A3-100991 · Drug

Registered with NAFDAC — registration activeAs of 6 November 2026 · synced automatically from official sources.
Product
Sukkar Blood Glucose Monitoring Device
NAFDAC number
A3-100991
Active ingredient
Blood Glucose Monitor
Strength
NA
Form
NA
Pack size
1 Bag
Manufacturer
Not listed
Applicant (holder)
Sepat Pharmaceuticals Ltd
Approved
9 Jul 2023
Status
Active View on NAFDAC ↗
Registration valid to
5 Jul 2028
WHO alerts
None found
Community reports
None
Times checked
0

RxVerify commentary

  • Sukkar Blood Glucose Monitoring Device is on the NAFDAC register with an active registration (A3-100991). 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. Not medical advice — always follow your doctor or pharmacist.

What Sukkar Blood Glucose Monitoring Device is used for

From the official U.S. FDA label for blood glucose monitor, the active ingredient registered with NAFDAC.

What it is used for

HCB-Res For the temporary relief of dizziness, weakness, and shortness of breath associated with heart irregularity and angina.

Purpose

HCB-Res Helps with circulatory system and blood.

Warnings

HCB-Res Use only under direction of a health care professional. Do not use if tamper evident seal is broken or missing.

General information only — not dosing advice. Always follow the leaflet in your pack and your doctor or pharmacist.

Check your pack of Sukkar Blood Glucose Monitoring Device

Add the expiry date printed on your pack for a full Trust Score — or look up uses, side effects and cheaper generics.

3 free checks left today · no signup Official sources: NAFDAC Green Book & recalls · WHO · U.S. FDA · NLM RxNorm

About Sukkar Blood Glucose Monitoring Device

What is in Sukkar Blood Glucose Monitoring Device?

Sukkar Blood Glucose Monitoring Device contains Blood Glucose Monitor (NA), as na, according to its NAFDAC registration record.

Is Sukkar Blood Glucose Monitoring Device registered with NAFDAC?

Yes. Sukkar Blood Glucose Monitoring Device is listed on the NAFDAC register under registration number A3-100991, and its registration is active as of 6 November 2026.

Has Sukkar Blood Glucose Monitoring Device been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Sukkar Blood Glucose Monitoring Device in our automatically synced alert list.

How can I check that my pack of Sukkar Blood Glucose Monitoring Device is genuine?

Run a free authenticity scan with the NAFDAC number A3-100991, 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.

What is Sukkar Blood Glucose Monitoring Device used for?

HCB-Res For the temporary relief of dizziness, weakness, and shortness of breath associated with heart irregularity and angina. (Summarised from the official U.S. FDA label for blood glucose monitor. Always follow your doctor or pharmacist.)

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