APO-GRANISETRON granisetron hydrochloride 3mg/3mL injection ampoule

Country: Australia

Language: English

Source: Department of Health (Therapeutic Goods Administration)

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Active ingredient:

granisetron hydrochloride, Quantity: 3.36 mg (Equivalent: granisetron, Qty 3 mg)

Available from:

Arrotex Pharmaceuticals Pty Ltd

INN (International Name):

granisetron hydrochloride

Pharmaceutical form:

Injection

Composition:

Excipient Ingredients: citric acid monohydrate; hydrochloric acid; sodium hydroxide; sodium chloride; water for injections

Administration route:

Intravenous

Units in package:

5

Prescription type:

(S4) Prescription Only Medicine

Therapeutic indications:

Adults: Granisetron Injection is indicated for use in adults for:,The prevention and treatment of nausea and vomiting induced by cytotoxic chemotherapy;,The prevention of nausea and vomiting induced by radiotherapy.,Granisetron Injection is also indicated for use in the prevention and treatment of post-operative nausea and vomiting.,Children: Granisetron injection is indicated for the prevention of nausea and vomiting induced by cytotoxic chemotherapy.

Product summary:

Visual Identification: Granisetron Hydrochloride Injection, 3mg/3mL is a clear and colorless solution, in a type 1 glass ampoule; Container Type: Ampoule; Container Material: Glass Type I Clear; Container Life Time: 24 Months; Container Temperature: Store below 25 degrees Celsius

Authorization status:

Registered

Authorization date:

2014-12-17