VERSATIS

This brand name is authorized in Austria, Ecuador, Estonia, Spain, France, Croatia, Ireland, Lithuania, Mexico, Netherlands, Poland, Romania, United Kingdom, South Africa

Active ingredients

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

1 Lidocaine UNII 98PI200987 - LIDOCAINE

Lidocaine, like other local anaesthetics, causes a reversible blockade of impulse propagation along nerve fibres by preventing the inward movement of sodium ions through the nerve membrane. Local anaesthetics of the amide-type are thought to act within the sodium channels of the nerve membrane. Read about Lidocaine

Medicine classification

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

ATC code	Group title	Classification
N01BB02	Lidocaine	N Nervous system → N01 Anesthetics → N01B Anesthetics, local → N01BB Amides
Discover more medicines within N01BB02

Authorization and marketing

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

Country	Identification scheme	Identifier(s)
Country: EC	Agencia Nacional de Regulación, Control y Vigilancia Sanitaria	Identifier(s): 27.909-12-07
Country: EE	Ravimiamet	Identifier(s): 1433090, 1433102, 1433113, 1433124, 1433135
Country: ES	Centro de información online de medicamentos de la AEMPS	Identifier(s): 34009, 3400938285673, 71848
Country: FR	Base de données publique des médicaments	Identifier(s): 65538840
Country: GB	Medicines & Healthcare Products Regulatory Agency	Identifier(s): 110527, 369026, 374472, 377083, 379738, 381731
Country: HR	Agencija za lijekove i medicinske proizvode	Identifier(s): HR-H-140669749
Country: IE	Health Products Regulatory Authority	Identifier(s): 11020, 30500
Country: LT	Valstybinė vaistų kontrolės tarnyba	Identifier(s): 1038830, 1058245, 1058246, 1058247, 1058248
Country: MX	Comisión Federal para la Protección contra Riesgos Sanitarios	Identifier(s): 166M
Country: NL	Z-Index G-Standaard, PRK	Identifier(s): 83372
Country: PL	Rejestru Produktów Leczniczych	Identifier(s): 100241048
Country: RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	Identifier(s): W64546001, W64546002, W64546003, W64546004, W64546005
Country: ZA	Health Products Regulatory Authority	Identifier(s): 43/3.2.3/0382