NDC 67296-2103
Terbinafine 250 mg tablet
On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from Aurobindo Pharma Limited's NDC 65862-079.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Medchal, India | Makes it and tests it | Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action |
Repackaging site
- RedPharm Drug, Eden Prairie, MN, United States · repackages it
Product details
- Generic drug
- Terbinafine: every company that makes it
- Form
- tablet
- Strength
- 250 mg
- Approval
- ANDA ANDA078297
- On the market since
- Jul 2, 2007
- Package NDCs
67296-2103-9- Official label
- DailyMed (National Library of Medicine), updated Jul 25, 2024
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