FLAREX

Google image searchProduct monograph

Active ingredient

fluorometholone acetate, 0.1 %/W/V

DIN: 00756784

Dosage form(s): SUSPENSION

Route(s) of administration: OPHTHALMIC

Schedule: Prescription

Company: NOVARTIS PHARMACEUTICALS CANADA INC

Date: 09-MAR-2018

ATC:

• S01 — OPHTHALMOLOGICALS (ATC, ATC/DDD, )
• S01B — ANTIINFLAMMATORY AGENTS (ATC, ATC/DDD)
• S01BA — Corticosteroids, plain (ATC, ATC/DDD)
• S01BA07 — FLUOROMETHOLONE (ATC/DDD)

Reference brand drug: Flarex, Fml

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Novartis Pharmaceuticals Canada Inc

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