TIMOPTOL

This brand name is authorized in Australia, Brazil, Ecuador, France, Hong Kong SAR China, Ireland, Italy, Japan, Mexico, New Zealand, Singapore, UK.

Active ingredients

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

1
UNII P8Y54F701R - TIMOLOL MALEATE
 

Timolol is a non-selective beta-adrenergic receptor blocking agent that does not have significant intrinsic sympathomimetic, direct myocardial depressant, or local anaesthetic activity. Timolol reduces intra-ocular pressure, whether or not this is associated with glaucoma.

 
Read more about Timolol

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 TIMOPTOL Eye drops, solution MPI, EU: SmPC Medicines & Healthcare Products Regulatory Agency (GB)

Medicine classification

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

ATC Group Classification
S01ED01 Timolol S Sensory organs → S01 Ophthalmologicals → S01E Antiglaucoma preparations and miotics → S01ED Beta blocking agents
Discover more medicines within S01ED01

Authorization and marketing

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

Country Identification scheme Identifier(s)
AU Pharmaceutical Benefits Scheme 1279H, 1926J, 5548B, 5550D
BR Câmara de Regulação do Mercado de Medicamentos 525502303171319, 525502304178317, 556718030001707, 556718030001807
EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria 24.057-1-09-11
FR Base de données publique des médicaments 60396928, 61417407, 64190637, 64342874
GB Medicines & Healthcare Products Regulatory Agency 146682, 146685, 14971, 15004, 162741, 162802, 34115, 34175
HK Department of Health Drug Office 02362
IE Health Products Regulatory Authority 74349, 74357
IT Agenzia del Farmaco 024278107, 024278121
JP 医薬品医療機器総合機構 1319702Q1107, 1319702Q2111, 1319702Q3037, 1319702Q4033
MX Comisión Federal para la Protección contra Riesgos Sanitarios 0313M79
NZ Medicines and Medical Devices Safety Authority 2749, 2750
SG Health Sciences Authority 04135P, 08619P

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