NDC 57237-098
Cefadroxil 500 mg per 5 mL powder, for suspension
On the label: Rising Pharma Holdings, Inc..
Where it's 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 |
Product details
- Generic drug
- Cefadroxil: every company that makes it
- Form
- powder, for suspension, oral
- Strength
- 500 mg per 5 mL
- Approval
- ANDA ANDA065349
- On the market since
- Apr 25, 2013
- Package NDCs
57237-098-0157237-098-75- Official label
- DailyMed (National Library of Medicine), updated Feb 9, 2024
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