NDC 53002-2654
Cefdinir 125 mg per 5 mL powder, for suspension
On the label: RPK Pharmaceuticals, Inc.. It's repackaged: RPK Pharmaceuticals, Inc. 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
- RPK Pharmaceuticals, Inc., Union City, California, United States · repackages it and relabels it
Product details
- Generic drug
- Cefdinir: every company that makes it
- Form
- powder, for suspension
- Strength
- 125 mg per 5 mL
- Approval
- ANDA ANDA065473
- On the market since
- Dec 14, 2007
- Package NDCs
53002-2654-153002-2654-2- Official label
- DailyMed (National Library of Medicine), updated Jan 31, 2023
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