

A clinical briefing on Natacyn (Natamycin) availability in 2026. Supply status, prescribing implications, alternatives, and tools for ophthalmology providers.
Natacyn (Natamycin ophthalmic suspension 5%) remains the sole FDA-approved topical antifungal for ophthalmic use in the United States. For providers managing fungal keratitis, conjunctivitis, and blepharitis, understanding the current supply landscape is essential to ensuring timely patient care.
This briefing covers the current availability picture, prescribing considerations, alternative therapies, cost and access challenges, and tools to help your patients find Natacyn in stock.
Natacyn has been available in the U.S. since its FDA approval in 1978. Manufactured exclusively by Alcon Laboratories (Fort Worth, Texas), it has remained a single-source branded product with no FDA-approved generic throughout its market history.
Key timeline points:
As of February 2026, Natacyn is not listed on the FDA Drug Shortage database. However, intermittent supply disruptions and limited retail pharmacy stocking continue to create access barriers for patients.
Natacyn is indicated for fungal blepharitis, conjunctivitis, and keratitis caused by susceptible organisms, including Fusarium solani, Aspergillus, Candida, Cephalosporium, and Penicillium.
Natamycin achieves therapeutic concentrations in the corneal stroma but demonstrates poor intraocular penetration. It is not effective as monotherapy for fungal endophthalmitis. Systemic absorption following topical ophthalmic administration is negligible.
If keratitis does not improve after 7-10 days of Natacyn therapy, consider that the causative organism may not be susceptible. Re-evaluate clinically and obtain additional cultures and sensitivity testing.
Despite no official shortage, providers should be aware of several practical access challenges:
Providers managing acute fungal keratitis should proactively address pharmacy availability at the time of prescribing rather than assuming the patient will be able to fill without difficulty.
The financial burden on patients is significant:
For patients facing cost barriers, providers should consider:
When Natacyn is unavailable or clinically suboptimal, the following compounded alternatives are widely used in ophthalmology practice:
Note: None of these alternatives are FDA-approved as ophthalmic formulations. Clinical judgment should guide selection based on culture results, infection severity, and patient factors.
To help your patients access Natacyn and navigate availability challenges:
For detailed workflow recommendations, see our companion guide: How to Help Your Patients Find Natacyn in Stock.
Several factors will shape Natacyn access going forward:
In the meantime, maintaining relationships with specialty pharmacies and compounding facilities ensures your practice can provide timely treatment regardless of Natacyn availability fluctuations.
Natacyn remains an essential medication in the ophthalmology armamentarium. While it is not in official shortage, the practical reality of limited stocking, single-source manufacturing, and high cost means providers must be proactive about access.
Key recommendations:
By anticipating access challenges and having contingency plans in place, providers can ensure that patients with fungal eye infections receive prompt, effective treatment.
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