NDC 68180-182
Cefadroxil 500 mg per 5 mL powder, for suspension
On the label: Lupin Pharmaceuticals, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lupin Limited | Mandideep, India | Makes it | Serious problems, FDA actionNov 23, 2022 · 6 inspections, 3 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 ANDA065396
- On the market since
- Apr 23, 2008
- Package NDCs
68180-182-0168180-182-0268180-182-03- Official label
- DailyMed (National Library of Medicine), updated Oct 8, 2025
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