NDC 68071-2683
Cefdinir 250 mg per 5 mL powder, for suspension
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Ascend Laboratories, LLC's NDC 67877-548.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Alkem Laboratories Limited | Amaliya Daman, India | Makes it, tests it and packages it | No problems foundAug 30, 2019 · 6 inspections |
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · relabels it
Product details
- Generic drug
- Cefdinir: every company that makes it
- Form
- powder, for suspension
- Strength
- 250 mg per 5 mL
- Approval
- ANDA ANDA210534
- On the market since
- Feb 20, 2021
- Package NDCs
68071-2683-1- Official label
- DailyMed (National Library of Medicine), updated Apr 28, 2022
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