NDC 68788-8115
cefdinir 125 mg per 5 mL powder, for suspension
On the label: Preferred Pharmaceuticals, Inc... It's repackaged: Preferred Pharmaceuticals, Inc.. rebottles it from Ascend Laboratories, LLC's NDC 67877-547.
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
- 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
- 125 mg per 5 mL
- Approval
- ANDA ANDA210534
- On the market since
- Dec 7, 2021
- Package NDCs
68788-8115-168788-8115-6- Official label
- DailyMed (National Library of Medicine), updated Mar 24, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?