NDC 73190-095
Deferiprone 500 mg tablet
On the label: AvKARE, Inc.. It's repackaged: AvKARE, Inc. rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 51672-4196.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Taro Pharmaceutical Industries Ltd. | Haifa Bay, Israel | Makes it | No problems foundDec 8, 2022 · 7 inspections |
Product details
- Generic drug
- Deferiprone: every company that makes it
- Form
- tablet, oral
- Strength
- 500 mg
- Approval
- ANDA ANDA208800
- On the market since
- Aug 12, 2026
- Package NDCs
73190-095-01- Official label
- DailyMed (National Library of Medicine), updated Aug 12, 2026
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