NDC 52652-9001
Eprontia 25 mg per 1 mL solution
On the label: Azurity Pharmaceuticals, Inc. (formerly Arbor Pharmaceuticals).
Where it's made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Azurity Pharmaceuticals, Inc. (formerly Arbor Pharmaceuticals) names for other drugs.
Recalls
- Dec 8, 2023 · Class III · Azurity Pharmaceuticals, Inc.
Failed Impurities/Degradation Specifications: Out of specification Impurity C (4,5-desisopropylidene topiramate) result observed during routine stability testing at 18 months.
Lots: Lot #: MB22020B, Exp 12/27/2023
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Topiramate: every company that makes it
- Form
- solution, oral
- Strength
- 25 mg per 1 mL
- Approval
- NDA NDA214679
- On the market since
- Dec 6, 2021
- Package NDCs
52652-9001-152652-9001-252652-9001-3- Official label
- DailyMed (National Library of Medicine), updated Nov 13, 2025
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