Flarex 1 mg/mL
fluorometholone acetate · SUSPENSION/ DROPS · Harrow Eye, LLC
No Recall History
Plain English
Flarex is a suspension/ drops containing fluorometholone acetate at 1 mg/mL, taken ophthalmic. Manufactured by Harrow Eye, LLC.
Key Facts
- Brand Name
- Flarex
- Generic Name
- fluorometholone acetate
- NDC Code (Product)
82667-010- Manufacturer
- Harrow Eye, LLC
- Strength
- 1 mg/mL
- Dosage Form
- SUSPENSION/ DROPS
- Route
- OPHTHALMIC
- Marketing Status
- Application #
- NDA019079
- Marketing Start
- 03/31/2025
Recall History
No Recall HistoryFrequently Asked Questions
What is Flarex used for?
Flarex contains fluorometholone acetate. It is a suspension/ drops taken ophthalmic. Consult your doctor for specific uses.
Is Flarex a controlled substance?
Flarex is not classified as a controlled substance by the DEA.
What is the generic name for Flarex?
The generic name for Flarex is fluorometholone acetate. There are no other listed brand versions of fluorometholone acetate.
What is the NDC code for Flarex 1 mg/mL?
The NDC (National Drug Code) for Flarex 1 mg/mL is 82667-010, listed by Harrow Eye, LLC.
Other Flarex Dosages
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)