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Vinorelbine Tartrate 10mg / ml injection

Ferron Par Pharmaceuticals

Product packaging may vary from one country to another.

Ingredients in every ml

Vinorelbine Tartrate 10 mg

Each package contains

1 vial of 1 ml

Other details

Dosage formInjection
Flavour None

W.H.O. classification

ATC Level 1 L - Antineoplastic and immunomodulating agents
ATC Level 2 L01 - Antineoplastic Agents
ATC Level 3 L01C - Plant Alkaloids and Other Natural Products; Antineoplastic Drugs



NOT RECOMMENDEDThis item is not safe for use during pregnancy.


NOT RECOMMENDEDThis item is not safe for use during lactation.


CONSULT YOUR DOCTORSafety of this item for use with alcohol has not been established. Please consult your doctor.


CAUTIONThis item may not be safe for use while operating heavy machinery. Use with caution and after consultation with your doctor.

Available in


Dosage information

Strictly by intravenous administration after appropriate dilution. The use of intrathecal route is contraindicated. It is recommended to infuse vinorelbine over 6-10 minutes after dilution in 20-50 ml of 0.9% NaCl Injection (normal saline solution) or 5% dextrose solution. Administration should always be followed with at least 250 ml of an isotonic solution infusion to flush the vein.

— In monotherapy:
The usual dose given is 25-30 mg/m² once weekly.

— In combination chemotherapy:
The dose may be the same while the frequency of administration reduced, i.e.: day 1 and 5 every 3 weeks or day 1 and 8 every 3 weeks according to treatment protocol.

No dose adjustments are required for renal insufficiency. If moderate or severe neurotoxicity develops, vinorelbine should be discontinued. The dosage should be adjusted according to hematologic toxicity or hepatic insufficiency, whichever results the lower dose.


Treatment of non-small cell lung cancer and advanced breast cancer in combination with standard chemotherapy.