NDC 72189-185
Cefdinir 125 mg per 5 mL powder, for suspension
On the label: Direct Rx. It's repackaged: Direct Rx rebottles it from Aurobindo Pharma Limited's NDC 65862-218.
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
- Direct Rx, Dawsonville, GA, 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 ANDA065473
- On the market since
- Apr 12, 2021
- Package NDCs
72189-185-32- Official label
- DailyMed (National Library of Medicine), updated Jan 22, 2025
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