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Irish Medicines Database · HPRA register

Famotidine 20 mg film-coated tablets

Authorisation PA1142/043/001 · Amdipharm Limited

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Famotidine 20 mg film-coated tablets
Licence PA1142/043/001 · Unknown
Licence holder
Amdipharm Limited (all products →)
Active substance
Famotidine
Dosage form
Film-coated tablet
Route of administration
Oral use
ATC code
A02BA03
First authorised
06/07/2026
Prescription status
Product subject to prescription which may be renewed (B)
Supply
Supply through pharmacies only
Legal basis
Generic application (Article 10(1) of Directive No 2001/83/EC)

Data: Health Products Regulatory Authority (HPRA) open dataset, licensed CC BY 4.0, published 16 Sep 2026. This listing is regulatory information, not medical advice — consult the package leaflet, SPC, or a healthcare professional. For the authoritative record see the HPRA register.