This brand name is authorized in Canada, Finland, Hong Kong, Ireland, Japan, New Zealand, Poland, Turkey, United Kingdom, United States
The drug KETALAR contains one active pharmaceutical ingredient (API):
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1
Ketamine
UNII O18YUO0I83 - KETAMINE HYDROCHLORIDE
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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. |
Below package inserts are available for further reading:
| Title | Information Source | Document Type | |
|---|---|---|---|
| KETALAR Solution for injection or infusion | Medicines & Healthcare Products Regulatory Agency (GB) | MPI, EU: SmPC |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC code | Group title | Classification |
|---|---|---|
| N01AX03 | Ketamine | N Nervous system → N01 Anesthetics → N01A Anesthetics, general → N01AX Other general anesthetics |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| Country: CA | Health Products and Food Branch | Identifier(s): 00224391, 00224405 |
| Country: FI | Lääkealan turvallisuus- ja kehittämiskeskus | Identifier(s): 150086 |
| Country: GB | Medicines & Healthcare Products Regulatory Agency | Identifier(s): 388043, 39890, 39907 |
| Country: HK | Department of Health Drug Office | Identifier(s): 07196, 07197, 07901 |
| Country: JP | 医薬品医療機器総合機構 | Identifier(s): 1119400A1031, 1119400A2038, 1119400A3026 |
| Country: NZ | Medicines and Medical Devices Safety Authority | Identifier(s): 1039 |
| Country: PL | Rejestru Produktów Leczniczych | Identifier(s): 100033210, 100033232 |
| Country: TR | İlaç ve Tıbbi Cihaz Kurumu | Identifier(s): 8681308771056 |
| Country: US | FDA, National Drug Code | Identifier(s): 42023-113, 42023-114, 42023-115, 52584-037 |
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