NDC 60687-275
Phenytoin 125 mg per 5 mL suspension
On the label: American Health Packaging. It's repackaged: American Health Packaging rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 51672-4069.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Taro Pharmaceutical Industries Ltd. | Haifa Bay, Israel | Makes it | No problems foundDec 8, 2022 · 7 inspections |
Repackaging site
- American Health Packaging, Columbus, OH, United States · repackages it
Recalls
- Feb 7, 2020 · Class I · Taro Pharmaceuticals U.S.A., Inc.
Resuspension Problems: Two lots of Phenytoin Oral Suspension USP 125mg/5mL may coagulate and may not resuspend as per the label copy instructions.
Lots: Lot# 327874, 327876, Exp Dec/2020
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Phenytoin: every company that makes it
- Form
- suspension, oral
- Strength
- 125 mg per 5 mL
- Approval
- ANDA ANDA040521
- On the market since
- Jan 10, 2019
- Package NDCs
60687-275-6260687-275-6360687-275-66- Official label
- DailyMed (National Library of Medicine), updated Sep 17, 2025
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