Ketamine Mylan

País: Nova Zelândia

Língua: inglês

Origem: Medsafe (Medicines Safety Authority)

Ingredientes ativos:

Ketamine hydrochloride 115.3 mg/mL equivalent to Ketamine 100 mg/mL

Disponível em:

Viatris Limited

DCI (Denominação Comum Internacional):

Ketamine hydrochloride 115.3 mg/mL (equivalent to Ketamine 100 mg/mL)

Dosagem:

200 mg/2mL

Forma farmacêutica:

Solution for injection

Composição:

Active: Ketamine hydrochloride 115.3 mg/mL equivalent to Ketamine 100 mg/mL Excipient: Benzethonium chloride Nitrogen Water for injection

Tipo de prescrição:

Class C4 Controlled Drug

Fabricado por:

CU Chemie Uetikon GmbH

Indicações terapêuticas:

Ketamine is indicated: · as the sole anaesthetic agent for diagnostic and surgical procedures that do not require skeletal muscle relaxation. Ketamine is best suited for short procedures and it can be used with additional doses' for longer procedures · for the induction of anaesthesia prior to the administration of other general anaesthetic agents · to supplement low-potency agents' such as nitrous oxide.

Resumo do produto:

Package - Contents - Shelf Life: Vial, glass, 2 mL Type 1 (USP) closed with bromobutyl rubber stopper and aluminium cap - 5 dose units - 24 months from date of manufacture stored at or below 25°C protect from light 24 hours diluted stored at 2° to 8°C (Refrigerate, do not freeze) protect from light. in 5% dextrose, 0.9% sodium chloride, or water for injection - Vial, glass, 2 mL Type 1 (USP) closed with bromobutyl rubber stopper and aluminium cap - 10 dose units - 24 months from date of manufacture stored at or below 25°C protect from light 24 hours diluted stored at 2° to 8°C (Refrigerate, do not freeze) protect from light. in 5% dextrose, 0.9% sodium chloride, or water for injection

Data de autorização:

2014-12-10