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Molecule

Interferon beta-1a

Interferon beta
Available on requestBiologicOrphanCold chainMultiple sclerosis
Presentations
9
Brands
4
Manufacturers
2
Available from stock
0

Interferon beta-1a is an interferon beta indicated for the treatment of relapsing forms of multiple sclerosis (MS), to include clinically isolated syndrome, relapsing-remitting disease, and active secondary progressive disease, in adults. MedsAcross supplies Interferon beta-1a for export from India to licensed hospitals, importers and physicians acting for named patients, with the documents each country requires.

Information from the US FDA prescribing information, retrieved 12 November 2026. Not yet medically reviewed.How we review

Key facts

Pharmacological class
Interferon beta
ATC classification
L03AB07 Interferon beta-1a · Interferon
US FDA first approval
17 May 1996
EU status
Authorised
Orphan designation
Yes
WHO essential medicine
Not recorded
India (CDSCO)
Not yet confirmed against CDSCO approval lists
Routes
Subcutaneous, Intramuscular
Dosage forms
Injection, Kit
Biologic
Yes
Identifiers
UNII XRO4566Q4RRxCUI 75917CAS 145258-61-3DrugBank DB00060Q2450337

Clinical information

From the regulator-approved product information. Each section names its source.

Uses

AVONEX is indicated for the treatment of relapsing forms of multiple sclerosis (MS), to include clinically isolated syndrome, relapsing-remitting disease, and active secondary progressive disease, in adults. AVONEX is for the treatment of relapsing forms of multiple sclerosis (MS), to include clinically isolated syndrome, relapsing-remitting disease, and active secondary progressive disease, in adults.

Source: US FDA prescribing information

How it works

The mechanism of action by which AVONEX exerts its effects in patients with multiple sclerosis is unknown.

Source: US FDA prescribing information

Dosing overview

For intramuscular use only. Recommended dose: 30 micrograms once a week. AVONEX may be titrated, starting with 7.5 micrograms for first week, to reduce flu-like symptoms. Increase dose by 7.5 micrograms each week for next 3 weeks until recommended dose of 30 micrograms. See patient instructions for use for complete administration instructions. Perform first injection under the supervision of an appropriately qualified health care professional. Analgesics and/or antipyretics on treatment days may help ameliorate flu-like symptoms

Source: US FDA prescribing information

Contraindications

AVONEX is contraindicated in patients with a history of hypersensitivity to natural or recombinant interferon beta, or any other component of the formulation. The formerly available lyophilized vial formulation of AVONEX is contraindicated in patients with a history of hypersensitivity to albumin (human). History of hypersensitivity to natural or recombinant interferon beta, albumin or any other component of the formulation

Source: US FDA prescribing information

Warnings and precautions

Depression, Suicide, and Psychotic Disorders: advise patients to immediately report any symptoms of depression, suicidal ideation, and/or psychosis, consider discontinuation of AVONEX if depression occurs. Hepatic Injury: monitor liver function tests, monitor patients for signs and symptoms of hepatic injury, consider discontinuation of AVONEX if hepatic injury occurs. Injection Site Reactions: Do not administer AVONEX into affected area until fully healed, if multiple lesions occur, change injection site or discontinue AVONEX until healing of skin lesions. Anaphylaxis and Other Allergic-Reactions: Discontinue if occurs. Congestive Heart Failure: monitor patients with pre-existing significant cardiac disease for worsening of cardiac symptoms. Decreased Peripheral Blood Counts: monitor complete blood count.

Source: US FDA prescribing information

Side effects

The following serious adverse reactions are discussed in more detail in other sections of labeling: Depression, Suicide, and Psychotic Disorders Hepatic Injury Anaphylaxis and Other Allergic-Reactions Injection Site Reactions Including Necrosis Congestive Heart Failure Decreased Peripheral Blood Counts Thrombotic Microangiopathy Pulmonary Arterial Hypertension Seizures Autoimmune Disorders Laboratory Tests The most common adverse reactions (at least 5% more frequent on AVONEX than on placebo) were flu-like symptoms including chills, fever, myalgia, and asthenia.

Source: US FDA prescribing information

Storage

Refrigerate AVONEX prefilled syringes and autoinjectors at 2°C to 8°C (36°F to 46°F) in the original carton to protect from light. DO NOT FREEZE. Once removed from the refrigerator, allow prefilled syringes and autoinjectors to warm to room temperature (about 30 minutes). Should refrigeration be unavailable, a prefilled syringe or autoinjector may be stored at room temperature up to 25°C (77°F) for a period up to 7 days. Once the product is removed from the refrigerator, it must not be stored above 25°C (77°F).

Source: US FDA prescribing information

For healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.

All presentations

9 presentations of Interferon beta-1a, sorted by availability.

MedicineManufacturerRegisterAvailability
Avonex kitIntramuscular Cold chainBiogenUS FDAAvailable on request
Avonex 30 mcg/0.5 mL injectionIntramuscular Cold chainBiogenUS FDAAvailable on request
Avonex Pen 30 mcg/0.5 mL injectionIntramuscular Cold chainBiogenUS FDAAvailable on request
Rebif kitSubcutaneous Cold chainEMD SeronoUS FDAAvailable on request
Rebif 22 mcg/0.5 mL injectionSubcutaneous Cold chainEMD SeronoUS FDAAvailable on request
Rebif 44 mcg/0.5 mL injectionSubcutaneous Cold chainEMD SeronoUS FDAAvailable on request
Rebif Rebidose kitSubcutaneous Cold chainEMD SeronoUS FDAAvailable on request
Rebif Rebidose 22 mcg/0.5 mL injectionSubcutaneous Cold chainEMD SeronoUS FDAAvailable on request
Rebif Rebidose 44 mcg/0.5 mL injectionSubcutaneous Cold chainEMD SeronoUS FDAAvailable on request

Brands by market

4 brand names across 1 markets.

Brand names by country

Manufacturers

Regulatory status

Approval facts from US FDA, EMA and CDSCO data, and registration status by country where we hold register data.

RegisterStatusSource
US FDAFirst approved 17 May 1996Drugs@FDA
EU (EMA)AuthorisedEMA medicines data
India (CDSCO)Not yet confirmed against CDSCO approval lists—
AustriaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
BelgiumRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
BulgariaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
CroatiaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
CyprusRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
CzechiaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
DenmarkRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
EstoniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
FinlandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
FranceRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
GermanyRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
GreeceRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
HungaryRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
IcelandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
IrelandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
ItalyRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LatviaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LiechtensteinRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LithuaniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LuxembourgRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
MaltaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
NetherlandsRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
NorwayRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
PolandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
PortugalRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
RomaniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SlovakiaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SloveniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SpainRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SwedenRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
United StatesRegisteredUS FDA (NDC directory, openFDA)Checked 12 November 2026

Conditions

Conditions linked to Interferon beta-1a in public data. This is not a list of approved uses, see the clinical information.

Questions and answers

Is Interferon beta-1a available for export from India?

Yes, on request. MedsAcross lists 9 presentations of Interferon beta-1a and sources them for licensed hospitals, importers and physicians against valid import documents.

What brand names does Interferon beta-1a have?

The catalogue lists 4 brand names for Interferon beta-1a, including Avonex, Avonex Pen, Rebif, Rebif Rebidose.

Is Interferon beta-1a approved by the US FDA?

Yes. The US FDA first approved Interferon beta-1a on 17 May 1996, according to Drugs@FDA.

Is Interferon beta-1a authorised in the European Union?

Yes. Interferon beta-1a has a central EU marketing authorisation (status: authorised), according to European Medicines Agency data.

Does Interferon beta-1a need cold chain shipping?

At least one listed presentation of Interferon beta-1a must be kept cold, so it is shipped in temperature-controlled packaging. Check the storage line on each presentation.

Which ATC class is Interferon beta-1a in?

Interferon beta-1a is classified under ATC code L03AB07 (Interferon beta-1a).

References

  1. Avonex prescribing information (Biogen). U.S. National Library of Medicine, DailyMed. Retrieved 19 November 2025
  2. Avonex: European public assessment report (EPAR). European Medicines Agency. Retrieved 26 May 2026
  3. Rebif: European public assessment report (EPAR). European Medicines Agency. Retrieved 2 September 2026

Request Interferon beta-1a for export supply

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