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Updated 04 Jul 2026 · HPRA open data

Actavis Group hf — Licensed Medicines

35 medicines held by Actavis Group hf on the Irish market, from the HPRA register of authorised products.

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
← All medicines · 35 products held by Actavis Group hf
MedicineActive substanceLicence holderStatus
Actelsar HCT 40 mg/12.5 mg tablets
EU/1/13/817/001-013
Hydrochlorothiazide, Telmisartan Actavis Group hf
Actelsar HCT 80 mg/12.5 mg tablets
EU/1/13/817/014-028
Hydrochlorothiazide, Telmisartan Actavis Group hf
Actelsar HCT 80 mg/25 mg tablets
EU/1/13/817/029-041
Hydrochlorothiazide, Telmisartan Actavis Group hf
Armisarte 25 mg/ml concentrate for solution for infusion
EU/1/15/1063/001-004
Pemetrexed diacid Actavis Group hf
Desloratadine Actavis 5 mg film-coated tablets
EU/1/11/745/001-009
Desloratadine Actavis Group hf
Ebilfumin 30 mg hard capsules
EU/1/14/915/001-002
Oseltamivir phosphate Actavis Group hf
Ebilfumin 45 mg hard capsules
EU/1/14/915/003-004
Oseltamivir phosphate Actavis Group hf
Ebilfumin 75 mg hard capsules
EU/1/14/915/005-006
Oseltamivir phosphate Actavis Group hf
Levetiracetam Actavis 1000 mg film-coated tablets
EU/1/11/713/031-040
Levetiracetam Actavis Group hf
Levetiracetam Actavis 250 mg film-coated tablets
EU/1/11/713/001-010
Levetiracetam Actavis Group hf
Levetiracetam Actavis 500 mg film-coated tablets
EU/1/11/713/011-020
Levetiracetam Actavis Group hf
Levetiracetam Actavis 750 mg film-coated tablets
EU/1/11/713/021-030
Levetiracetam Actavis Group hf
Levetiracetam Actavis Group 100 mg/ml oral solution
EU/1/11/738/001-003
Levetiracetam Actavis Group hf
Nemdatine 10 mg film-coated tablets
EU/1/13/824/003-010
Memantine hydrochloride Actavis Group hf
Nemdatine 15 mg film-coated tablets
EU/1/13/824/011-013
Memantine hydrochloride Actavis Group hf
Nemdatine 20 mg film-coated tablets
EU/1/13/824/014-017
Memantine hydrochloride Actavis Group hf
Nemdatine 5 mg film-coated tablets
EU/1/13/824/001-002
Memantine hydrochloride Actavis Group hf
Nemdatine 5 mg, 10 mg, 15 mg, 20 mg film-coated tablets
EU/1/13/824/018
Memantine hydrochloride, Memantine hydrochloride, Memantine hydrochloride, Memantine hydrochloride Actavis Group hf
Pioglitazone Actavis 15 mg tablets
EU/1/12/755/001-009
Pioglitazone hydrochloride Actavis Group hf
Pioglitazone Actavis 30 mg tablets
EU/1/12/755/010-018
Pioglitazone hydrochloride Actavis Group hf
Pioglitazone Actavis 45 mg tablets
EU/1/12/755/019-027
Pioglitazone hydrochloride Actavis Group hf
Potactasol 1 mg powder for concentrate for solution for infusion
EU/1/10/660/001
Topotecan hydrochloride Actavis Group hf
Potactasol 4 mg powder for concentrate for solution for infusion
EU/1/10/660/002
Topotecan hydrochloride Actavis Group hf
Rapilysin 10 U powder and solvent for solution for injection.
EU/1/96/018/001
Reteplase Actavis Group hf
Rivastigmine Actavis 1.5 mg hard capsules
EU/1/11/693/001-004
Rivastigmine hydrogen tartrate Actavis Group hf
Rivastigmine Actavis 3 mg hard capsules
EU/1/11/693/005-008
Rivastigmine hydrogen tartrate Actavis Group hf
Rivastigmine Actavis 4.5 mg hard capsules
EU/1/11/693/009-012
Rivastigmine hydrogen tartrate Actavis Group hf
Rivastigmine Actavis 6 mg hard capsules
EU/1/11/693/013-016
Rivastigmine hydrogen tartrate Actavis Group hf
Sildenafil Actavis 100 mg film-coated tablets
EU/1/09/595/11-15
Sildenafil Actavis Group hf
Sildenafil Actavis 25 mg film-coated tablets
EU/1/09/595/1-5
Sildenafil Actavis Group hf
Sildenafil Actavis 50 mg film-coated tablets
EU/1/09/595/6-10
Sildenafil Actavis Group hf
Telmisartan Actavis 20 mg tablets
EU/1/10/639/001-010
Telmisartan Actavis Group hf
Telmisartan Actavis 40 mg tablets
EU/1/10/639/011-020
Telmisartan Actavis Group hf
Telmisartan Actavis 80 mg tablets
EU/1/10/639/021-030
Telmisartan Actavis Group hf
Zoledronic acid Actavis 4 mg/5 ml concentrate for solution for infusion
EU/1/12/759/001-003
Zoledronic acid monohydrate Actavis Group hf
Cite this database

Priya Life Science (2026). Irish Medicines Database. Available at: https://priyalifescience.com/medicines (Accessed: 20 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.