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Difalabs Ject

NAFDAC Reg. No. A3-100558 · Drug

Registered with NAFDAC. Registration activeAs of 29 October 2026 · synced automatically from official sources.
Product
Difalabs Ject
NAFDAC number
A3-100558
Active ingredient
Syringes and Needles
Strength
NA
Form
NA
Pack size
2 mL x 100; 5 mL x 100
Manufacturer
Not listed
Applicant (holder)
Divine Favour Medical Laboratories
Approved
23 Dec 2021
Status
Active View on NAFDAC ↗
Registration valid to
13 Dec 2026
WHO alerts
None found
Community reports
None
Times checked
0

About the medicine: Syringes: uses, dosage and brands worldwide

What we found

  • Difalabs Ject is on the NAFDAC register with an active registration (A3-100558). 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 Difalabs Ject

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

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3 free checks left today Official sources: U.S. FDA · EMA (EU) · NAFDAC · WHO alerts

About Difalabs Ject

What is in Difalabs Ject?

Difalabs Ject contains Syringes and Needles (NA), as na, according to its NAFDAC registration record.

Is Difalabs Ject registered with NAFDAC?

Yes. Difalabs Ject is listed on the NAFDAC register under registration number A3-100558, and its registration is active as of 29 October 2026.

Has Difalabs Ject been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Difalabs Ject in our automatically synced alert list.

How can I check that my pack of Difalabs Ject is genuine?

Run a free authenticity scan with the NAFDAC number A3-100558, 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.