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Priya Life Science Medicines register
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Registers› Irish medicines
Medicines register · Ireland

Every medicine authorised for the Irish market

The Health Products Regulatory Authority's full list of authorised products — brand, active substance, licence holder, licence number and market status. Filter it, cite it, and take it away as a file.

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Source: HPRA open dataset ("Authorised or Transfer Pending Products"), CC BY 4.0. Complete coverage — all 10,336 authorised products are in this register. Synced 20 Sep 2026, 17:51 UTC
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Matches brand name, active substance, licence holder and licence number.
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89 of 10,336 medicines
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Medicine
Active substance
Licence holder
Status
Actos EU/1/00/150/011
Pioglitazone
Takeda Pharma A/S
—
ADCETRIS 50 mg powder for concentrate for solution for infusion EU/1/12/794/001
Brentuximab vedotin
Takeda Pharma A/S
—
Advate 1000 IU/2 ml powder and solvent for solution for injection EU/1/03/271/009
Recombinant coagulation fviii (octocog alfa)
Takeda Manufacturing Austria AG
—
Advate 1000 IU/5 ml powder and solvent for solution for injection EU/1/03/271/003
Recombinant coagulation fviii (octocog alfa)
Takeda Manufacturing Austria AG
—
Advate 1500 IU/5 ml powder and solvent for solution for injection EU/1/03/271/004
Recombinant coagulation fviii (octocog alfa)
Takeda Manufacturing Austria AG
—
Advate 2000 IU/5 ml powder and solvent for solution for injection EU/1/03/271/005
Recombinant coagulation fviii (octocog alfa)
Takeda Manufacturing Austria AG
—
Advate 250 IU/2 ml powder and solvent for solution for injection EU/1/03/271/007
Recombinant coagulation fviii (octocog alfa)
Takeda Manufacturing Austria AG
—
Advate 250 IU/5 ml powder and solvent for solution for injection EU/1/03/271/001
Recombinant coagulation fviii (octocog alfa)
Takeda Manufacturing Austria AG
—
Advate 3000 IU/5 ml powder and solvent for solution for injection EU/1/03/271/006
Recombinant coagulation fviii (octocog alfa)
Takeda Manufacturing Austria AG
—
Advate 500 IU/2 ml powder and solvent for solution for injection EU/1/03/271/008
Recombinant coagulation fviii (octocog alfa)
Takeda Manufacturing Austria AG
—
Advate 500 IU/5 ml powder and solvent for solution for injection EU/1/03/271/002
Recombinant coagulation fviii (octocog alfa)
Takeda Manufacturing Austria AG
—
ADZYNMA 1500 IU powder and solvent for solution for injection EU/1/24/1837/002
Apadamtase alfa
Takeda Manufacturing Austria AG
—
ADZYNMA 500 IU powder and solvent for solution for injection EU/1/24/1837/001
Apadamtase alfa
Takeda Manufacturing Austria AG
—
Alunbrig 180 mg film-coated tablets EU/1/18/1264/009-010
Brigatinib
Takeda Pharma A/S
—
Alunbrig 30 mg film-coated tablets EU/1/18/1264/001-004
Brigatinib
Takeda Pharma A/S
—
Alunbrig 90 mg film-coated tablets EU/1/18/1264/005-008
Brigatinib
Takeda Pharma A/S
—
Cinryze 500 IU powder and solvent for solution for injection EU/1/11/688/001
C1 inhibitor
Takeda Manufacturing Austria AG
—
CONTROLOC Control 20 mg Gastro-resistant tablet EU/1/09/515/001-004
Pantoprazole sodium sesquihydrate
Takeda GmbH
—
Dengue Tetravalent Vaccine (Live, Attenuated) Takeda EU/1/22/1699/001
Dengue virus serotype 1# (live, attenuated), Dengue virus, serotype 2, live, attenuated, Dengue virus serotype 3# (live, attenuated), Dengue virus serotype 4# (live, attenuated)
Takeda GmbH
—
Dengue Tetravalent Vaccine (Live, Attenuated) Takeda EU/1/22/1699/002
Dengue virus serotype 1# (live, attenuated), Dengue virus, serotype 2, live, attenuated, Dengue virus serotype 3# (live, attenuated), Dengue virus serotype 4# (live, attenuated)
Takeda GmbH
—
Dengue Tetravalent Vaccine (Live, Attenuated) Takeda EU/1/22/1699/003
Dengue virus serotype 1# (live, attenuated), Dengue virus, serotype 2, live, attenuated, Dengue virus serotype 3# (live, attenuated), Dengue virus serotype 4# (live, attenuated)
Takeda GmbH
—
Dengue Tetravalent Vaccine (Live, Attenuated) Takeda EU/1/22/1699/004
Dengue virus serotype 1# (live, attenuated), Dengue virus, serotype 2, live, attenuated, Dengue virus serotype 3# (live, attenuated), Dengue virus serotype 4# (live, attenuated)
Takeda GmbH
—
Deqsiga 100 mg/mL solution for infusion/human normal immunoglobulin (IVIg) EU/1/25/1919/001-002
Human Normal Immunoglobulin (IV)
Takeda Manufacturing Austria AG
—
Edarbi 20 mg tablets EU/1/11/734/001-004
Azilsartan medoxomil
Takeda Pharma A/S
—
Edarbi 40 mg tablets EU/1/11/734/005-008
Azilsartan medoxomil
Takeda Pharma A/S
—
Edarbi 80 mg tablets EU/1/11/734/009-011
Azilsartan medoxomil
Takeda Pharma A/S
—
Elaprase 2 mg/ml concentrate for solution for infusion EU/1/06/365/1-3
Idursulfase
Takeda Pharmaceuticals International AG Ireland Branch
—
Entyvio 108 mg solution for injection in pre-filled pen EU/1/14/923/005-007
Vedolizumab
Takeda Pharma A/S
—
Entyvio 108 mg solution for injection in pre-filled syringe EU/1/14/923/002-004
Vedolizumab
Takeda Pharma A/S
—
Entyvio 300 mg powder for concentrate for solution for infusion EU/1/14/923/001
Vedolizumab
Takeda Pharma A/S
—
Equasym XL 10 mg modified-release capsules, hard PA23211/001/001
Methylphenidate hydrochloride
Takeda Pharmaceuticals International AG Ireland Branch
Marketed
Equasym XL 20 mg modified-release capsules, hard PA23211/001/002
Methylphenidate hydrochloride
Takeda Pharmaceuticals International AG Ireland Branch
Marketed
Equasym XL 30 mg modified-release capsules, hard PA23211/001/003
Methylphenidate hydrochloride
Takeda Pharmaceuticals International AG Ireland Branch
Marketed
Equasym XL 40 mg modified-release capsules, hard PA23211/001/004
Methylphenidate hydrochloride
Takeda Pharmaceuticals International AG Ireland Branch
Not marketed
Equasym XL 50 mg modified-release capsules, hard PA23211/001/005
Methylphenidate hydrochloride
Takeda Pharmaceuticals International AG Ireland Branch
Not marketed
Equasym XL 60 mg modified-release capsules, hard PA23211/001/006
Methylphenidate hydrochloride
Takeda Pharmaceuticals International AG Ireland Branch
Not marketed
Firazyr 30 mg solution for injection in pre-filled syringe EU/1/08/461/001-002
Icatibant
Takeda Pharmaceuticals International AG Ireland Branch
—
Foznol 1000 mg Chewable Tablets PA23211/002/004
Lanthanum
Takeda Pharmaceuticals International AG Ireland Branch
Marketed
Foznol 1000 mg Oral Powder PA23211/002/006
Lanthanum carbonate hydrate
Takeda Pharmaceuticals International AG Ireland Branch
Not marketed
Foznol 250 mg Chewable Tablets PA23211/002/001
Lanthanum carbonate hydrate
Takeda Pharmaceuticals International AG Ireland Branch
Not marketed
Foznol 500 mg Chewable Tablets PA23211/002/002
Lanthanum
Takeda Pharmaceuticals International AG Ireland Branch
Marketed
Foznol 750 mg Chewable Tablets PA23211/002/003
Lanthanum
Takeda Pharmaceuticals International AG Ireland Branch
Marketed
Foznol 750 mg Oral Powder PA23211/002/005
Lanthanum carbonate hydrate
Takeda Pharmaceuticals International AG Ireland Branch
Not marketed
Incresync 12.5 mg/30 mg film-coated tablets EU/1/13/842/01-09
Alogliptin (as benzoate), Pioglitazone (as hydrochloride)
Takeda Pharma A/S
—
Incresync 12.5 mg/45 mg film-coated tablets EU/1/13/842/010-018
Alogliptin (as benzoate), Pioglitazone (as hydrochloride)
Takeda Pharma A/S
—
Incresync 25 mg/30 mg film-coated tablets EU/1/13/842/019-027
Pioglitazone (as hydrochloride), Alogliptin (as benzoate)
Takeda Pharma A/S
—
Incresync 25 mg/45 mg film-coated tablets EU/1/13/842/028-036
Pioglitazone (as hydrochloride), Alogliptin (as benzoate)
Takeda Pharma A/S
—
Intuniv 1 mg prolonged-release tablets EU/1/15/1040/001-002
GUANFACINE HYDROCHLORIDE
Takeda Pharmaceuticals International AG Ireland Branch
—
Intuniv 2 mg prolonged-release tablets EU/1/15/1040/003-005
GUANFACINE HYDROCHLORIDE
Takeda Pharmaceuticals International AG Ireland Branch
—
Intuniv 3 mg prolonged-release tablets EU/1/15/1040/006-007
GUANFACINE HYDROCHLORIDE
Takeda Pharmaceuticals International AG Ireland Branch
—
Showing 1–50 of 89
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Cite this view

Priya Life Science (2026). Irish Medicines Register, filtered. Derived from the HPRA open dataset. Retrieved 28 September 2026. https://priyalifescience.com/medicines

Download this register
GET /api/export.php?register=medicines-ie&format=csv Try the JSON export →
Regulatory information only — not medical advice. For the authoritative record see the HPRA register directly.