

A provider briefing on Eprontia availability in 2026. Understand the supply landscape, prescribing implications, alternatives, and tools to help patients.
Eprontia (Topiramate oral solution, 25 mg/mL) is the first and only FDA-approved ready-to-use liquid formulation of Topiramate. Since its approval in November 2021, it has become an important option for patients who require or prefer a liquid anticonvulsant — particularly pediatric patients, those with dysphagia, and individuals on feeding tubes.
However, many providers have encountered patient complaints about difficulty filling Eprontia prescriptions. This briefing covers the current supply landscape, prescribing considerations, cost and access factors, and practical tools to support your patients.
Eprontia is not currently listed on the FDA Drug Shortage Database as of early 2026. Unlike some anticonvulsants that have experienced manufacturing-related shortages, Eprontia's availability challenges are structural rather than supply-driven:
The core issue is not a manufacturing shortfall but rather limited distribution to retail pharmacies, driven by the product's niche demand and cost profile.
When prescribing Eprontia, consider the following clinical and logistical factors:
Eprontia carries the same indications as other Topiramate formulations:
Topiramate carries significant reproductive safety concerns. Data show a 2- to 5-fold increase in the risk of oral clefts (cleft lip/palate) in infants exposed to Topiramate during the first trimester. Additionally, infants may be born small for gestational age (SGA). Women of childbearing potential should use effective contraception while taking any Topiramate formulation, including Eprontia.
Providers should be aware of significant interactions, detailed further in our drug interactions guide:
The reality on the ground is that most retail pharmacies do not stock Eprontia. Key factors include:
Understanding the cost picture helps when counseling patients:
To help your patients access Eprontia efficiently:
Several developments may improve Eprontia access over the coming years:
In the meantime, providers can help by educating patients about availability tools, cost-saving programs, and — when Eprontia is unavailable — appropriate alternative formulations.
Eprontia fills an important clinical niche as the only FDA-approved liquid Topiramate. While it is not in a formal shortage, practical availability remains limited. By understanding the supply dynamics, leveraging tools like Medfinder for Providers, and connecting patients with savings programs, you can minimize treatment interruptions and ensure continuity of care.
For patient-facing resources, refer patients to: How to Find Eprontia in Stock Near You and How to Save Money on Eprontia.
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