NDC 70518-2749
Cefixime 400 mg capsule
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. 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 29, 2021 · Class II · RemedyRepack Inc.
Failed Impurities/Degradation Specifications
Lots: Lot #: a) B1429436-110821, Exp 07/2022; B1429434-110821, Exp 11/2022; B1429435-110821, Exp 11/2022; B1279449-072021, Exp 07/2022; B1279457-072021, Exp 07/2022; B1279442-072021,Exp 07/2022; B1057718-012621, Exp 01/2022; B1057727-012621, Exp 01/2022; b) B1358139-092121, Exp 03/2022; B1424654-110421… - 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
- May 21, 2020
- Package NDCs
70518-2749-070518-2749-170518-2749-270518-2749-370518-2749-470518-2749-5- Official label
- DailyMed (National Library of Medicine), updated Jul 28, 2026
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