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Tamiflu

Oseltamivir

An oral antiviral medication used to treat and prevent influenza A and B.

Neuraminidase inhibitor
Generic name
Oseltamivir
Brand name
Tamiflu
Route
Oral
Marketed by
Roche
First FDA approval
27 Oct 1999

Where Oseltamivir is approved

All regulators →

Of the three regulators tracked here, the first to approve Oseltamivir was the US, on 27 Oct 1999. It is approved in 3 of the 3 regulators tracked here.

USUnited States (FDA)
27 Oct 1999
Tamiflu
NDA021087 on Drugs@FDA
First original NDA/BLA approval
EUEuropean Union (EMA)
20 Jun 2002
Tamiflu
EMA product page
First centralised authorisation
CACanada (Health Canada)
23 Dec 1999
Tamiflu
Notice of Compliance 1971
First new-drug NOC

From the regulators' own registers: FDA Drugs@FDA, the EMA medicines list and Health Canada's Notice of Compliance database. Dates are the first listed approval of a product containing only this substance; combination products and nationally authorised EU medicines are not counted.

What health systems spend on Oseltamivir

All medicines →
ENNHS England
£502k
37,167 items dispensed, Aug 2025 to Jul 2026
+2% on the previous 12 months
Net ingredient cost, community prescriptions
USUS Medicaid
$59.7m
2,420,600 prescriptions in 2025 · Oseltamivir phosphate, Oseltamivir Phosphate, oseltamivir phosphate
+36% on 2024
Amount Medicaid reimbursed, before rebates

From NHSBSA Prescription Cost Analysis (Open Government Licence v3.0) and CMS State Drug Utilization Data. Both are gross amounts: neither system publishes its discounts or rebates per drug. Products combining several substances are not counted here.

How Oseltamivir works

All drug targets →
  • Neuraminidase inhibitor Inhibitor
    ChEMBL only
Diseases it has been tested for in clinical trials, by furthest phase
  • COVID-19Phase 3
  • COVID-19–associated multisystem inflammatory syndrome in childrenPhase 3
  • Orthocoronavirinae infectious diseasePhase 3
  • Autoimmune thrombocytopenic purpuraPhase 3
  • Influenza A (H1N1)Phase 3
  • Swine influenzaPhase 3
  • Recurrent lower respiratory tract infectionsPhase 2
  • InfectionPhase 2
  • PneumoniaPhase 2

Mechanisms and diseases from ChEMBL via the Open Targets Platform (release 26.09), ChEMBL record CHEMBL1229, CC BY-SA 3.0. Targets checked against the IUPHAR/BPS Guide to PHARMACOLOGY (2026.3), ligand 11427, CC BY-SA 4.0. Trial phases are not approvals: approved uses are shown from the regulators' own records where we hold them.

NICE appraisals of Oseltamivir

All NICE appraisals →

NICE, which decides whether the NHS in England should fund new medicines, has published 4 technology appraisals of Oseltamivir. 4 are current, and 4 of these recommend it for at least some patients.

AppraisalNICE recommendationPublishedStatus
Amantadine, oseltamivir and zanamivir for the treatment of influenza
NICE TA168
Recommended Not recommended25 Feb 2009Current
Oseltamivir, amantadine (review) and zanamivir for the prophylaxis of influenza
NICE TA158
Not recommended Recommended24 Sep 2008Current
The clinical effectiveness and cost effectiveness of amantadine and oseltamivir for the prophylaxis of influenza
NICE TA67
Not recommended Recommended24 Sep 2003Current
Flu treatment - zanamivir, amantadine and oseltamivir
NICE TA58
Not recommended Recommended26 Feb 2003Current

NICE decisions apply to the NHS in England. In Ireland the HSE decides on reimbursement, advised by the National Centre for Pharmacoeconomics. Titles, categories and dates link to the guidance on nice.org.uk. © NICE 2026 technology appraisal guidance. Available from www.nice.org.uk/guidance. All rights reserved. Subject to Notice of rights. NICE guidance is prepared for the National Health Service in England. All NICE guidance is subject to regular review and may be updated or withdrawn. NICE accepts no responsibility for the use of its content in this product/publication.

Patient leaflets for Oseltamivir

The package leaflet is the official guide for patients that comes with every medicine. These links go to the regulators that publish it.

  • IE
    Ireland: 7 products on the HPRA list
    Each product record links to the HPRA, which publishes the leaflet and SmPC.
  • EU
    European Union: Tamiflu, Ebilfumin (generic)
    EMA product information: package leaflet and summary of product characteristics in every EU language.
  • UK
    United Kingdom: Search MHRA Products
    Patient information leaflets and SmPCs for UK-licensed products.
  • US
    United States: Search DailyMed
    FDA-approved labels, including patient and medication guides.

Leaflets differ between brands and countries; always read the one that comes with your own medicine. This is regulatory information, not medical advice.

Reference identifiers for Oseltamivir

ATC code
J05AH02
ChEMBL
CHEMBL1229
DrugBank
DB00198
PubChem CID
65028
CAS number
196618-13-0
FDA UNII
20O93L6F9H
Wikidata
Q211509
Wikipedia
Oseltamivir

Codes that identify this medicine in other databases, from Wikidata (CC0), matched by its ChEMBL ID. The ATC code is the WHO classification of what the medicine is used for.

What Tamiflu is used for

TAMIFLU is an influenza neuraminidase inhibitor (NAI) indicated for: Treatment of acute, uncomplicated influenza A and B in patients 2 weeks of age and older who have been symptomatic for no more than 48 hours. ( 1.1 ) Prophylaxis of influenza A and B in patients 1 year and older. ( 1.2 ) Limitations of Use : Not a substitute for annual influenza vaccination. ( 1.3 ) Consider available information on influenza drug susceptibility patterns and treatment effects when deciding whether to use. ( 1.3 ) Not recommended for patients with end-stage renal disease not undergoing dialysis. ( 1.3 ) 1.1 Treatment of Influenza TAMIFLU is indicated for the treatment of acute, uncomplicated illness due to influenza A and B infection in patients 2 weeks of age and older who have been symptomatic for no more than 48 hours. 1.2 Prophylaxis of Influenza TAMIFLU is indicated for the prophylaxis of influenza…

How it works

12.1 Mechanism of Action Oseltamivir is an antiviral drug with activity against influenza virus [see Microbiology (12.4) ].

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How this page is built

The facts on this page are pulled directly from official U.S. FDA datasets — they are not written from memory. Each field below names the dataset it came from, so you can check it yourself.

Plain-English summaries and drug-class explainers are written and reviewed by Sreepriya Prasannan (MSc Digital Transformation of Life Sciences (Innopharma Education / Griffith College); MSc & BSc Botany). Data is retrieved automatically from the sources above and cross-checked with AI-assisted verification (Anthropic's Claude) — brand and generic names are matched against the exact FDA product record so that a combination product or a different formulation cannot be mistaken for the drug on this page. An editor reviews the result before publication. We describe this in full in our editorial standards and corrections policy. The FDA data on this page was last retrieved on 11 Oct 2026. How every register is built: methodology · fixes we have made: corrections log.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician — our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us — we correct promptly and log it.