NDC 83112-400
Cefixime 400 mg 400 mg capsule
On the label: Health Department, Oklahoma State. It's repackaged: Health Department, Oklahoma State rebottles it from Ascend Laboratories, LLC's NDC 67877-584.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Alkem Laboratories Limited | Amaliya Daman, India | Makes it | No problems foundAug 30, 2019 · 6 inspections |
Recalls
- Dec 21, 2021 · Class II · Ascend Laboratories, LLC
Failed impurities/degradation specifications
Lots: Lot #: 20140293, Exp Dec 2021; 20141525, 20141526, 20141527, Exp Mar 2022; 20143019, 20143020, 20143021, 20143022, Exp July 2022; 20144759, 20144760, 20144761, Exp Nov 22 - Nov 3, 2021 · Class II · Ascend Laboratories LLC
Failed Impurities/Degradation Specifications
Lots: Lot 20140282, exp Dec 2021
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Cefixime: every company that makes it
- Form
- capsule, oral
- Strength
- 400 mg
- Approval
- ANDA ANDA210574
- On the market since
- Oct 12, 2018
- Package NDCs
83112-400-0083112-400-02- Official label
- DailyMed (National Library of Medicine), updated Dec 20, 2025
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