Zenapax 25 mg/5 ml Injection

Regulated Product — Business License Required

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Product Overview

Zenapax 25 mg/5 ml Injection contains daclizumab, an interleukin-2 receptor antagonist monoclonal antibody. Its labelling describes it for the treatment of multiple sclerosis (MS), a condition in which the immune system attacks the protective sheath around nerves. It is described as suppressing the immune response to reduce nerve inflammation and the risk of disease progression, and is given only by a healthcare professional.

Active ingredient
Daclizumab
Strength
25 mg / 5 ml
Dosage form
Solution for injection
Therapeutic class
Interleukin-2 receptor antagonist (monoclonal antibody) — immunomodulator
Regulatory status
Prescription / regulated — confirmed per enquiry and destination market
Availability
Confirmed per enquiry

Product Information

The following description reflects information associated with daclizumab and this product’s labelling. It has not been independently clinically verified by SDO Pharma and is provided for business and product-identification purposes only. It is not medical advice and does not replace the manufacturer’s official prescribing information.

Described Uses

  • Described for the treatment of multiple sclerosis
  • Described as suppressing the immune response that damages the protective sheath around nerves
  • Described as reducing nerve inflammation, limiting further nerve damage, and stabilising the immune system
Note: SDO Pharma has not independently verified the manufacturer’s efficacy claims for this product and makes no additional medical or clinical claims beyond what is described here. We do not claim FDA, UAE, EU, or other specific regulatory approval for this product unless independently verified. This is a prescription / regulated-status product; patient dispensing is the responsibility of the licensed business customer, not SDO Pharma.

Described Dosage & Administration

  • Administered only by a doctor or nurse as an injection — not self-administered
  • The doctor’s instructions on how to take it should be followed; if none are given, the label should be read
  • The stated dose should not be exceeded, as overdosing is described as causing serious side effects

Described Side Effects

Commonly described side effects include:

  • Upper respiratory tract infection and bronchitis
  • Flu-like symptoms
  • Dermatitis and eczema
  • Low or depressed mood
  • Injection-site reactions (pain, swelling, redness)

These are described as commonly temporary. Any severe, persistent, or unexpected reaction requires prompt medical attention.

Precautions

  • The doctor should be informed of all other medicines being taken
  • The doctor should be told if the recipient is pregnant or breastfeeding
  • Full medical records should be shared with the healthcare team before administration
  • Any persistent or severe side effect should be reviewed by a clinician

This summary is provided for informational purposes only and does not replace the manufacturer’s official product labelling or professional medical advice.

B2B, Import & Export

B2B, Import & Export Enquiries

SDO Pharma supports business enquiries for pharmaceutical products, including bulk and export supply, subject to applicable licensing, regulatory, import, and export requirements. Requirements vary according to the destination market and the nature of the transaction.

We do not claim that this product is available for import into every country, and we do not claim FDA, UAE, EU, or other specific regulatory approval unless independently verified. Applicable documentation — including a valid Drug License, tax registration, and Importer Exporter Code (IEC) where relevant — is discussed directly with our team as part of the enquiry process. This is a regulated / prescription-status product supplied only to licensed and authorized business customers; SDO Pharma does not sell it directly to individual patients or consumers. See our Regulated Products Policy.

Product Enquiry

Request Product Information

Interested in this product for your business? Submit your enquiry and our team will contact you regarding bulk supply, documentation, and applicable requirements.

Frequently Asked Questions

Per its labelling it contains daclizumab and is used for the treatment of multiple sclerosis, described as suppressing the immune response that damages the protective sheath around nerves. SDO Pharma has not independently verified the manufacturer’s claims and does not claim any specific regulatory approval unless independently confirmed.

Its labelling states it is administered by a doctor or nurse as an injection. It is not self-administered, and the stated dose should not be exceeded.

Licensed and authorized business customers can submit the product enquiry form above or contact our team directly. Product availability, documentation, and supply arrangements are confirmed per enquiry.

Availability depends on the destination market’s regulatory requirements and cannot be confirmed without a direct enquiry. See our B2B, Import & Export Enquiries section above.

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