OxyContin 20 mg prolonged release tablets | medicines.ie

Company: Mundipharma Pharmaceuticals Limited - Formerly Napp Laboratories
Active Ingredient: Oxycodone Hydrochloride
Strength: Oxycodone Hydrochloride: 20 mg
Dosage Form: Prolonged-release tablet
Legal Category: A - prescription, may not be renewed
Last Updated: 25/09/2026

Licence numbers with strength, ATC code and dosage form
Licence number	Strength	ATC Code	Dosage Form
PA1688/005/003	20 mg	N02AA05	Prolonged-release tablet

Licence number: PA1688/005/003
Strength: 20 mg
ATC Code: N02AA05
Dosage Form: Prolonged-release tablet

Mundipharma Pharmaceuticals Limited - Formerly Napp Laboratories

United Drug House Magna Drive, Magna Business Park, Citywest Road, Dublin 24, Ireland

Telephone: +441748828867
Email: medicalinformation@mundipharma.ie