OPATANOL

This brand name is authorized in Austria, Croatia, Cyprus, Estonia, Finland, France, Ireland, Italy, Lithuania, Netherlands, Nigeria, Poland, Romania, Spain, Tunisia, UK.

Active ingredients

The drug OPATANOL contains one active pharmaceutical ingredient (API):

1
UNII 2XG66W44KF - OLOPATADINE HYDROCHLORIDE
 

Olopatadine is a potent selective antiallergic/antihistaminic agent that exerts its effects through multiple distinct mechanisms of action.

 
Read more about Olopatadine

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 OPATANOL Eye drops, solution MPI, EU: SmPC European Medicines Agency (EU)

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC Group Classification
S01GX09 Olopatadine S Sensory organs → S01 Ophthalmologicals → S01G Decongestants and antiallergics → S01GX Other antiallergics
Discover more medicines within S01GX09

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country Identification scheme Identifier(s)
EE Ravimiamet 1140220, 1140231
ES Centro de información online de medicamentos de la AEMPS 02217001, 02217001IP2, 02217001IP3
FI Lääkealan turvallisuus- ja kehittämiskeskus 007921
FR Base de données publique des médicaments 66097007
GB Medicines & Healthcare Products Regulatory Agency 45329
IE Health Products Regulatory Authority 37412, 69324, 69339, 69340
IT Agenzia del Farmaco 035723016, 035723028, 048632018
LT Valstybinė vaistų kontrolės tarnyba 1030315, 1064140
NG Registered Drug Product Database A4-2926
Switch country to Nigeria in order to find specific presentations of OPATANOL
NL Z-Index G-Standaard 14812266
NL Z-Index G-Standaard, PRK 67563
PL Rejestru Produktów Leczniczych 100118477
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W64476001, W64476002
TN Direction de la Pharmacie et du Médicament 1903071, 20833021

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