PRILOTEKAL

This brand name is authorized in Netherlands, Poland, United Kingdom

Active ingredients

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

1 Prilocaine UNII MJW015BAPH - PRILOCAINE HYDROCHLORIDE

Prilocaine is a toluidine derivative and intermediate-acting amino amide with local anesthetic property. Prilocaine binds to the intracellular surface of sodium channels which blocks the subsequent influx of sodium into the cell. Action potential propagation and never function is, therefore, prevented. This block is reversible and when the drug diffuses away from the cell, sodium channel function is restored and nerve propagation returns. Read about Prilocaine

Medication package inserts

Below package inserts are available for further reading:

Title	Information Source	Document Type
PRILOTEKAL Solution for injection	Medicines & Healthcare Products Regulatory Agency (GB)	MPI, EU: SmPC

Medicine classification

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

ATC code	Group title	Classification
N01BB04	Prilocaine	N Nervous system → N01 Anesthetics → N01B Anesthetics, local → N01BB Amides
Discover more medicines within N01BB04

Authorization and marketing

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

Country	Identification scheme	Identifier(s)
Country: GB	Medicines & Healthcare Products Regulatory Agency	Identifier(s): 171903
Country: NL	Z-Index G-Standaard, PRK	Identifier(s): 106852
Country: PL	Rejestru Produktów Leczniczych	Identifier(s): 100317432