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Irish Medicines Database · HPRA register

BYANNLI 1 000 mg prolonged-release suspension for injection in pre-filled syringe

Authorisation EU/1/20/1453/008 · Janssen-Cilag International NV

← All medicines

BYANNLI 1 000 mg prolonged-release suspension for injection in pre-filled syringe

Licence EU/1/20/1453/008 · Unknown

Licence holder: Janssen-Cilag International NV (all products →)
Active substance: Paliperidone palmitate
Dosage form: Prolonged-release suspension for injection
Route of administration: Intramuscular use
ATC code: N05AX13
First authorised: 22/11/2021
Prescription status: Product subject to prescription which may not be renewed (A)
Supply: Supply through pharmacies only
Legal basis: Informed consent application (Article 10c of Directive No 2001/83/EC)

Data: Health Products Regulatory Authority (HPRA) open dataset, licensed CC BY 4.0, published 04 Jul 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.