TETRALYSAL

This brand name is authorized in Brazil, Ecuador, Finland, France, Hong Kong SAR China, Ireland, Malta, New Zealand, Poland, South Africa, Tunisia, UK.

Active ingredients

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

1
Lymecycline
UNII 7D6EM3S13P - LYMECYCLINE
 

Tetracyclines provide bacteriostatic action at the available plasma and tissue concentrations and are effective against intracellular and extracellular organisms. Their mechanism of action is based on an inhibition of ribosomal protein synthesis.

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 TETRALYSAL Hard capsule 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
J01AA04 Lymecycline J Antiinfectives for systemic use → J01 Antibacterials for systemic use → J01A Tetracyclines → J01AA Tetracyclines
Discover more medicines within J01AA04

Authorization and marketing

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

Country Identification scheme Identifier(s)
BR Câmara de Regulação do Mercado de Medicamentos 510101702115311, 510101703111318, 510101704118413
EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria 24.399-04-02, 25.618-04-04
FI Lääkealan turvallisuus- ja kehittämiskeskus 002422, 012831, 157016
FR Base de données publique des médicaments 60061171, 60891060
GB Medicines & Healthcare Products Regulatory Agency 21562, 73359
HK Department of Health Drug Office 06231
IE Health Products Regulatory Authority 13214, 78305, 78308, 78357
MT Medicines Authority AA117/00703, AA908/25101
NZ Medicines and Medical Devices Safety Authority 253
PL Rejestru Produktów Leczniczych 100110665, 100174872, 100240020, 100330987, 100335571, 100462892
TN Direction de la Pharmacie et du Médicament 7393101
ZA Health Products Regulatory Authority E/20.1.1/67

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