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Drug company (FDA labeler)

Harrow Eye, LLC

NDC labeler codes: 73521, 82667

What is a labeler?

The company whose name is on the package and in the FDA’s National Drug Code (NDC) Directory. It may make the medicine itself or sell medicine made by another company. The first part of every NDC code identifies the labeler.

Official FDA data only

Products, approvals and recalls come from the FDA (NDC Directory, Drugs@FDA, enforcement reports). Recalls are linked to this company by the NDC labeler code on the recalled product.

Questions about your medicine: ask your doctor or pharmacist. In an emergency, call 911.

At a glance

17Products (NDC)

Prescription medicines

FDA applications for these products

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
  • BLA: Biologics License Application: how a biologic medicine (made from living cells) is approved.
ApprovedApplicationMedicineSponsor
March 4, 2024NDA218158 Clobetasol propionate
BYQLOVI
Harrow Eye
May 30, 2023NDA217469 Cyclosporine
VEVYE
Harrow Eye
September 27, 2022NDA216227 Chloroprocaine hydrochloride
IHEEZO
Harrow Eye
October 15, 2021NDA213978 Varenicline tartrate
TYRVAYA
Harrow Eye
September 17, 2021BLA761202 Ranibizumab-eqrn
BYOOVIZ
Samsung Bioepis Co Ltd
June 23, 2021NDA214965 Cyclosporine
VERKAZIA
Harrow Eye
May 30, 2017NDA208694 Cetirizine
ZERVIATE
Harrow Eye
October 16, 2012NDA203491 Nepafenac
ILEVRO
Harrow Eye
February 13, 2009NDA050818 Tobramycin and dexamethasone
TOBRADEX ST
Harrow Eye
November 29, 2007NDA022048 Triamcinolone acetonide
TRIESENCE
Harrow Eye
August 19, 2005NDA021862 Nepafenac
NEVANAC
Harrow Eye
April 15, 2003NDA021598 Moxifloxacin
VIGAMOX
Harrow Eye
December 31, 1987NDA019779 Apraclonidine hydrochloride ophthalmic solution
IOPIDINE
Harrow Eye
February 11, 1986NDA019079 Fluorometholone acetate
FLAREX
Harrow Eye
October 30, 1978NDA050514 Natamycin
NATACYN
Harrow Eye
June 6, 1963NDA050023 Neomycin sulfate, polymyxin b sulfate and dexamethasone
MAXITROL
Harrow Eye
June 20, 1962NDA013422 Dexamethasone
MAXIDEX
Harrow Eye

The sponsor is the company that holds the FDA application; it can differ from the labeler.

Recall timeline

No recall of these products (by NDC code) appears in the FDA enforcement reports.

Sources

  1. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  2. Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026

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