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Updated 04 Jul 2026 · HPRA open data

Irish Medicines Database

Every medicine authorised for the Irish market — 10,165 products with active substances, licence holders, dosage forms and prescription status.

A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 0–9
491 results for “Novo”
MedicineActive substanceLicence holderStatus
NovoNorm 2 mg tablets
EU/1/98/076/021
Repaglinide Novo Nordisk A/S
NovoRapid 100 U/ml Solution for injection
EU/1/99/119/001
Insulin aspart Novo Nordisk A/S
NovoRapid FlexPen 100 U/ml Solution for injection
EU/1/99/119/009-011
Insulin aspart Novo Nordisk A/S
NovoRapid FlexTouch 100 U/ml Solution for injection
EU/1/99/119/019
Insulin aspart Novo Nordisk A/S
NovoRapid InnoLet 100 U/ml Solution for injection
EU/1/99/119/012-014
Insulin aspart Novo Nordisk A/S
NovoRapid Penfill 100 U/ml Solution for injection
EU/1/99/119/003
Insulin aspart Novo Nordisk A/S
NovoRapid PumpCart 100 U/ml Solution for injection
EU/1/99/119/024-025
Insulin aspart Novo Nordisk A/S
NovoSeven (400 KIU)
EU/1/96/006/007
Eptacog alfa (activated) Novo Nordisk A/S
NovoSeven (100 KIU)
EU/1/96/006/005
Eptacog alfa (activated) Novo Nordisk A/S
NovoSeven (100 KIU)
EU/1/96/006/009
Eptacog alfa (activated) Novo Nordisk A/S
NovoSeven (250 KIU)
EU/1/96/006/006
Eptacog alfa (activated) Novo Nordisk A/S
NovoSeven (250 KIU)
EU/1/96/006/010
Eptacog alfa (activated) Novo Nordisk A/S
Novoseven (400 KIU)
EU/1/96/006/011
Eptacog alfa (activated) Novo Nordisk A/S
NovoSeven (50 KIU)
EU/1/96/006/004
Eptacog alfa (activated) Novo Nordisk A/S
NovoSeven (50 KIU)
EU/1/96/006/008
Eptacog alfa (activated) Novo Nordisk A/S
NovoThirteen 2500 IU powder and solvent for solution for injection
EU/1/12/775/001
Rfxiii drug substance Novo Nordisk A/S
Olmesartan Krka 10 mg film-coated tablets
PA1347/060/001
Olmesartan medoxomil KRKA, d.d., Novo mesto Marketed
Olmesartan Krka 20 mg film-coated tablets
PA1347/060/002
Olmesartan medoxomil KRKA, d.d., Novo mesto Marketed
Olmesartan Krka 40 mg film-coated tablets
PA1347/060/003
Olmesartan medoxomil KRKA, d.d., Novo mesto Marketed
Olmesartan medoxomil/Amlodipine/Hydrochlorothiazide Krka 40 mg/10 mg/25 mg film-coated tablets
PA1347/096/005
Olmesartan medoxomil, Amlodipine, Hydrochlorothiazide KRKA, d.d., Novo mesto Not marketed
Olmesartan medoxomil/Amlodipine/Hydrochlorothiazide Krka 40 mg/5 mg/12.5 mg film-coated tablets
PA1347/096/002
Olmesartan medoxomil, Amlodipine, Hydrochlorothiazide KRKA, d.d., Novo mesto Not marketed
Olmesartan medoxomil/Amlodipine/Hydrochlorothiazide Krka 40 mg/5 mg/25 mg film-coated tablets
PA1347/096/003
Olmesartan medoxomil, Amlodipine, Hydrochlorothiazide KRKA, d.d., Novo mesto Not marketed
Olmesartan medoxomil/Amlodipine/Hydrochlorothiazide Krka 20 mg/5 mg/12.5 mg film-coated tablets
PA1347/096/001
Olmesartan medoxomil, Amlodipine, Hydrochlorothiazide KRKA, d.d., Novo mesto Not marketed
Olmesartan medoxomil/Amlodipine/Hydrochlorothiazide Krka 40 mg/10 mg/12.5 mg film-coated tablets
PA1347/096/004
Olmesartan medoxomil, Amlodipine, Hydrochlorothiazide KRKA, d.d., Novo mesto Not marketed
Olmesartan/Amlodipine Krka 20 mg/5 mg film-coated tablets
PA1347/075/001
Olmesartan medoxomil, Amlodipine KRKA, d.d., Novo mesto Marketed
Olmesartan/Amlodipine Krka 40 mg/10 mg film-coated tablets
PA1347/075/003
Olmesartan medoxomil, Amlodipine KRKA, d.d., Novo mesto Marketed
Olmesartan/Amlodipine Krka 40 mg/5 mg film-coated tablets
PA1347/075/002
Olmesartan medoxomil, Amlodipine KRKA, d.d., Novo mesto Marketed
Olmesartan/Hydrochlorothiazide Krka 20 mg/12.5 mg film-coated tablets
PA1347/061/001
Olmesartan medoxomil, Hydrochlorothiazide KRKA, d.d., Novo mesto Marketed
Olmesartan/Hydrochlorothiazide Krka 20 mg/25 mg film-coated tablets
PA1347/061/002
Olmesartan medoxomil, Hydrochlorothiazide KRKA, d.d., Novo mesto Marketed
Olmesartan/Hydrochlorothiazide Krka 40 mg/12.5 mg film-coated tablets
PA1347/061/003
Olmesartan medoxomil, Hydrochlorothiazide KRKA, d.d., Novo mesto Marketed
Olmesartan/Hydrochlorothiazide Krka 40 mg/25 mg film-coated tablets
PA1347/061/004
Olmesartan medoxomil, Hydrochlorothiazide KRKA, d.d., Novo mesto Marketed
Oprymea 0.088 mg tablets
EU/1/08/469/1-5
Pramipexole KRKA, d.d., Novo mesto
Oprymea 0.18 mg tablets
EU/1/08/469/6-10
Pramipexole KRKA, d.d., Novo mesto
Oprymea 0.26 mg prolonged-release tablets
EU/1/08/469/026-029
Pramipexole KRKA, d.d., Novo mesto
Oprymea 0.35 mg tablets
EU/1/08/469/11-15
Pramipexole KRKA, d.d., Novo mesto
Oprymea 0.52 mg prolonged-release tablets
EU/1/08/469/030-033
Pramipexole KRKA, d.d., Novo mesto
Oprymea 0.7 mg tablets
EU/1/08/469/16-20
Pramipexole KRKA, d.d., Novo mesto
Oprymea 1.05 mg prolonged-release tablets
EU/1/08/469/034-037
Pramipexole KRKA, d.d., Novo mesto
Oprymea 1.1 mg tablets
EU/1/08/469/21-25
Pramipexole KRKA, d.d., Novo mesto
Oprymea 1.57 mg prolonged-release tablets
EU/1/08/469/038-041
Pramipexole KRKA, d.d., Novo mesto
Oprymea 2.1 mg prolonged-release tablets
EU/1/08/469/042-045
Pramipexole KRKA, d.d., Novo mesto
Oprymea 2.62 mg prolonged-release tablets
EU/1/08/469/046-049
Pramipexole dihydrochloride monohydrate KRKA, d.d., Novo mesto
Oprymea 3.15 mg prolonged-release tablets
EU/1/08/469/050-053
Pramipexole dihydrochloride monohydrate KRKA, d.d., Novo mesto
Ozempic 0.25 mg solution for injection in pre-filled pen
EU/1/17/1251/002
Semaglutide Novo Nordisk A/S
Ozempic 0.5 mg solution for injection in pre-filled pen
EU/1/17/1251/003-004
Semaglutide Novo Nordisk A/S
Ozempic 0.5 mg solution for injection in pre-filled pen
EU/1/17/1251/012-013
Semaglutide Novo Nordisk A/S
Ozempic 1 mg solution for injection in pre-filled pen
EU/1/17/1251/005-006
Semaglutide Novo Nordisk A/S
Ozempic 2 mg solution for injection in pre-filled pen
EU/1/17/1251/010-011
Semaglutide Novo Nordisk A/S
Paglitaz
EU/1/11/721/001-007
Pioglitazone hydrochloride KRKA, d.d., Novo mesto
Paglitaz
EU/1/11/721/008-014
Pioglitazone hydrochloride KRKA, d.d., Novo mesto
3 4 5 6 7 8 9
Cite this database

Priya Life Science (2026). Irish Medicines Database. Available at: https://priyalifescience.com/medicines (Accessed: 19 August 2026).

Data: Health Products Regulatory Authority (HPRA) open dataset (“Authorised or Transfer Pending Products”), licensed CC BY 4.0, refreshed daily. Regulatory information only — not medical advice.