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Name of the product: DREICO
Active ingredient: Zoledronic acid 4 mg
Dosage form: lyophilised injection
Dispensing requirements: Rx only
Argentine Industry
Composition:
Each glass bottle with lyophilised injection contains zoledronic acid 4 mg, mannitol and sodium citrate.
Each glass bottle with dissolving solution contains water for injection.
Indications:
DREICO is indicated for the treatment of malignant neoplastic hypercalcemia, and multiple myeloma and bone metastasis of solid tumours with conventional antineoplastic therapy.
Therapeutic action:
Osteoclastic resorption inhibitor.
Storage:
Keep at room temperature below 30º C in the marketed packing.
Marketed presentations:
Packs containing 1 glass bottle with lyophilised injection + 1 glass bottle with dissolving solution.
Packs containing 25 glass bottles with lyophilised injection + 25 glass bottles with dissolving solution, 50 glass bottles with lyophilised injection + 50 glass bottles with dissolving solution, and 100 glass bottles with lyophilised injection + 100 glass bottles with dissolving solution, for use in hospitals.
Medicinal speciality authorised by the Ministry of Health.
Certificate Nº 54144
Laboratorio DOSA S.A.
Girardot 1369, (C1427AKC) Buenos Aires, Argentine
Pharmaceutical Director: María C. Terzo, Pharmacist
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