Class III ยท Low risk
Zarontin (ethosuximide capsules, USP)
Labeling: Incorrect or Missing Lot and/or Exp Date. The expiry date on the product label is incorrect. The label states an expiry date of 09/2021 when it should be 09/2020.
National Drug Code
Is NDC 0071-0237-24 recalled?
Zarontin · 100 CAPSULE in 1 BOTTLE (0071-0237-24)
Yes — this exact package was recalled
1 FDA recall names the code 0071-0237-24 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
- Ethosuximide
- Strength
- ETHOSUXIMIDE 250 mg/1
- Form
- Capsule · Oral
- Labeler
- Parke-Davis Div of Pfizer Inc
- Type
- Human Prescription Drug
- Product code
- 0071-0237
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.
Other recalled products from this labeler
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