NDC 68788-7844
Cefdinir 250 mg per 5 mL powder, for suspension
On the label: Preferred Pharmaceuticals, Inc... It's repackaged: Preferred 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
- Preferred Pharmaceuticals Inc., Anaheim, 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
- Jan 20, 2021
- Package NDCs
68788-7844-1- Official label
- DailyMed (National Library of Medicine), updated Mar 24, 2026
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