Class III ยท Low risk
Eprontia (topiramate)
Failed Impurities/Degradation Specifications: Out of specification Impurity C (4,5-desisopropylidene topiramate) result observed during routine stability testing at 18 months.
National Drug Code
Is NDC 52652-9001-01 recalled?
Eprontia · 473 mL in 1 BOTTLE (52652-9001-1)
Yes — this exact package was recalled
1 FDA recall names the code 52652-9001-01 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- Topiramate
- Strength
- TOPIRAMATE 25 mg/mL
- Form
- Solution · Oral
- Labeler
- Azurity Pharmaceuticals, Inc.
- Type
- Human Prescription Drug
- Product code
- 52652-9001
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Free recall alerts
Know the day your medication is recalled
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