KEITA

This brand name is authorized in Nigeria.

Active ingredients

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

1	Ketamine UNII O18YUO0I83 - KETAMINE HYDROCHLORIDE
	Ketamine is a rapidly acting general anaesthetic for intravenous or intramuscular use with a distinct pharmacological action. Ketamine hydrochloride produces dissociative anaesthesia characterised by catalepsy, amnesia, and marked analgesia which may persist into the recovery period.
	Read more about Ketamine

Packages

This drug has been approved in Nigeria as follows:

Identifier	Form	Presentation	Description	Approval
C4-1983	Solution for injection	Keita Injection INJ_SOL 500 mg/10 mL 1 X 10VIALS	Solution for injection in a labelled vial containing ketamine anaesthetics.	26/05/2022

Medicine classification

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

ATC Group		Classification
N01AX03	Ketamine	N Nervous system → N01 Anesthetics → N01A Anesthetics, general → N01AX Other general anesthetics
Discover more medicines within N01AX03

Authorization and marketing

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

Country	Identification scheme	Identifier(s)
NG	Registered Drug Product Database	C4-1983