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Tetanus Antitoxin (Equine) for Human Use Injection

NAFDAC Reg. No. A6-100064 · Drug

Registered with NAFDAC. Registration activeAs of 27 October 2026 · synced automatically from official sources.
Product
Tetanus Antitoxin (Equine) for Human Use Injection
NAFDAC number
A6-100064
Active ingredient
Tetanus antitoxin
Strength
1500 IU/0.75 mL
Form
Solution for injection
Pack size
0.75 mL x 10's (in ampoules)
Manufacturer
Not listed
Applicant (holder)
Manfes Pharmaceutical Company Limited
Approved
17 Dec 2022
Status
Active View on NAFDAC ↗
Registration valid to
16 Dec 2027
WHO alerts
None found
Community reports
None
Times checked
0

What we found

  • Tetanus Antitoxin (Equine) for Human Use Injection is on the NAFDAC register with an active registration (A6-100064). 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.

What Tetanus Antitoxin (Equine) for Human Use Injection is used for

From the official U.S. FDA label for tetanus antitoxin, the active ingredient registered with NAFDAC.

What it is used for

• For the temporary relief of symptoms including: • cough • fever • congestion These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Purpose

Aconitum Napellus - Cough, Antimonium Tartaricum - Congestion, Bryonia (Alba) - Fever, Hyoscyamus Niger - Cough, Ipecacuanha - Cough, Kreosotum - Congestion, Pertussinum - Fever, Phosphorus - Congesti …

Warnings

If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away. Tamper Evident: Sealed for your protection. Do not use if 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 Tetanus Antitoxin (Equine) for Human Use Injection

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 Tetanus Antitoxin (Equine) for Human Use Injection

What is in Tetanus Antitoxin (Equine) for Human Use Injection?

Tetanus Antitoxin (Equine) for Human Use Injection contains Tetanus antitoxin (1500 IU/0.75 mL), as solution for injection, according to its NAFDAC registration record.

Is Tetanus Antitoxin (Equine) for Human Use Injection registered with NAFDAC?

Yes. Tetanus Antitoxin (Equine) for Human Use Injection is listed on the NAFDAC register under registration number A6-100064, and its registration is active as of 27 October 2026.

Has Tetanus Antitoxin (Equine) for Human Use Injection been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Tetanus Antitoxin (Equine) for Human Use Injection in our automatically synced alert list.

How can I check that my pack of Tetanus Antitoxin (Equine) for Human Use Injection is genuine?

Run a free authenticity scan with the NAFDAC number A6-100064, 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 Tetanus Antitoxin (Equine) for Human Use Injection used for?

• For the temporary relief of symptoms including: • cough • fever • congestion These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration. (Summarised from the official U.S. FDA label for tetanus antitoxin. Always follow your doctor or pharmacist.)

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