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Updated 04 Jul 2026 · HPRA open data

Novartis Ireland Limited — Licensed Medicines

47 medicines held by Novartis Ireland Limited 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 · 47 products held by Novartis Ireland Limited
MedicineActive substanceLicence holderStatus
Cataflam 50mg Coated Tablets
PA0896/004/001
Diclofenac potassium Novartis Ireland Limited Marketed
Certican 0.25mg Tablets
PA0896/005/001
Everolimus Novartis Ireland Limited Not marketed
Certican 0.75mg Tablets
PA0896/005/003
Everolimus Novartis Ireland Limited Not marketed
Ciloxan 3 mg/ml ear drops, solution
PA0896/006/001
Ciprofloxacin Novartis Ireland Limited Marketed
Co-Diovan 160 mg/12.5 mg film-coated tablets
PA0896/007/002
Valsartan, Hydrochlorothiazide Novartis Ireland Limited Marketed
Co-Diovan 160 mg/25 mg film-coated tablets
PA0896/007/003
Valsartan, Hydrochlorothiazide Novartis Ireland Limited Marketed
Co-Diovan 320 mg/12.5 mg film-coated tablets
PA0896/007/004
Valsartan, Hydrochlorothiazide Novartis Ireland Limited Marketed
Co-Diovan 320 mg/25 mg film-coated tablets
PA0896/007/005
Valsartan, Hydrochlorothiazide Novartis Ireland Limited Marketed
Co-Diovan 80 mg/12.5 mg film-coated tablets
PA0896/007/001
Valsartan, Hydrochlorothiazide Novartis Ireland Limited Marketed
Diovan 160 mg film-coated tablets
PA0896/009/002
Valsartan Novartis Ireland Limited Marketed
Diovan 320 mg film-coated tablets
PA0896/009/004
Valsartan Novartis Ireland Limited Marketed
Diovan 3mg/ml oral solution
PA0896/009/005
Valsartan Novartis Ireland Limited Marketed
Diovan 40 mg film-coated tablets
PA0896/009/003
Valsartan Novartis Ireland Limited Marketed
Diovan 80 mg film-coated tablets
PA0896/009/001
Valsartan Novartis Ireland Limited Marketed
Femara 2.5 mg film-coated tablets
PA0896/012/001
Letrozole Novartis Ireland Limited Not marketed
Lamisil 250 mg tablets
PA0896/015/001
Terbinafine Novartis Ireland Limited Not marketed
Lioresal 10 mg Tablets
PA0896/017/001
Baclofen Novartis Ireland Limited Marketed
Lioresal 5mg/5ml Oral solution
PA0896/017/002
Baclofen Novartis Ireland Limited Marketed
Luxturna 5 × 1012 vector genomes/mL concentrate and solvent for solution for injection
EU/1/18/1331/001
VORETIGENE NEPARVOVEC Novartis Ireland Limited
Maxidex 0.1% w/v Eye Drops, Suspension
PA0896/018/001
Dexamethasone Novartis Ireland Limited Marketed
Maxitrol 0.1% w/v, 6000 IU/ml, 3500 IU/ml eye drops, suspension
PA0896/019/001
Dexamethasone, Polymyxin b sulfate, Neomycin sulfate Novartis Ireland Limited Not marketed
Myfortic 180 mg gastro-resistant tablets
PA0896/023/001
Mycophenolic acid Novartis Ireland Limited Marketed
Myfortic 360 mg gastro-resistant tablets
PA0896/023/002
Mycophenolic acid Novartis Ireland Limited Marketed
Neoral 100 mg/ml concentrate for oral solution
PA0896/024/004
Ciclosporin Novartis Ireland Limited Marketed
Neoral 100mg Soft Capsules
PA0896/024/003
Ciclosporin Novartis Ireland Limited Marketed
Neoral 25 mg Soft Capsules
PA0896/024/001
Ciclosporin Novartis Ireland Limited Marketed
Neoral 50mg Soft Capsules
PA0896/024/002
Ciclosporin Novartis Ireland Limited Marketed
Sandimmun 50 mg/ml Concentrate for Solution for Infusion
PA0896/027/002
Ciclosporin Novartis Ireland Limited Marketed
SANDOSTATIN 100 microgram/1ml, solution for injection/infusion
PA0896/028/002
Octreotide Novartis Ireland Limited Marketed
SANDOSTATIN 50 microgram/1 ml, solution for injection/infusion
PA0896/028/001
Octreotide Novartis Ireland Limited Marketed
SANDOSTATIN 500 microgram/1 ml, solution for injection/infusion
PA0896/028/003
Octreotide Novartis Ireland Limited Marketed
Sandostatin LAR 10 mg powder and solvent for suspension for injection
PA0896/028/004
Octreotide Novartis Ireland Limited Marketed
Sandostatin LAR 20 mg powder and solvent for suspension for injection
PA0896/028/005
Octreotide Novartis Ireland Limited Marketed
Sandostatin LAR 30 mg powder and solvent for suspension for injection
PA0896/028/006
Octreotide Novartis Ireland Limited Marketed
Tegretol 100mg Tablets
PA0896/030/002
Carbamazepine Novartis Ireland Limited Marketed
Tegretol 100mg/5ml Oral Suspension
PA0896/030/001
Carbamazepine Novartis Ireland Limited Marketed
Tegretol 200mg Tablets
PA0896/030/003
Carbamazepine Novartis Ireland Limited Marketed
Tegretol 400mg Tablets
PA0896/030/004
Carbamazepine Novartis Ireland Limited Marketed
Tegretol SR 200mg prolonged release tablets
PA0896/030/005
Carbamazepine Novartis Ireland Limited Marketed
Tegretol SR 400mg prolonged release tablets
PA0896/030/006
Carbamazepine Novartis Ireland Limited Marketed
Trileptal 150 mg Film-coated tablets
PA0896/033/001
Oxcarbazepine Novartis Ireland Limited Marketed
Trileptal 300 mg Film-coated tablets
PA0896/033/002
Oxcarbazepine Novartis Ireland Limited Marketed
Trileptal 60 mg/ml Oral Suspension
PA0896/033/004
Oxcarbazepine Novartis Ireland Limited Marketed
Trileptal 600 mg Film-coated tablets
PA0896/033/003
Oxcarbazepine Novartis Ireland Limited Marketed
Voltarol 50 mg Gastro-Resistant Tablets
PA0896/034/001
Diclofenac sodium Novartis Ireland Limited Marketed
Voltarol Retard 100 mg Film-coated Prolonged Release Tablets
PA0896/034/002
Diclofenac sodium Novartis Ireland Limited Marketed
Voltarol Retard 75 mg Film-coated Prolonged-release Tablets
PA0896/034/003
Diclofenac sodium Novartis Ireland Limited Marketed
Cite this database

Priya Life Science (2026). Irish Medicines Database. Available at: https://priyalifescience.com/medicines (Accessed: 13 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.