NDC 68071-5106
Cefdinir 250 mg per 5 mL powder, for suspension
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Aurobindo Pharma Limited's NDC 65862-219.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Sangareddy, India | Makes it and tests it | Problems found, fixed voluntarilySep 29, 2023 · 5 inspections, 1 with FDA action |
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, oral
- Strength
- 250 mg per 5 mL
- Approval
- ANDA ANDA065473
- On the market since
- Dec 14, 2007
- Package NDCs
68071-5106-6- Official label
- DailyMed (National Library of Medicine), updated Jun 19, 2024
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