NDC 71205-061
Terbinafine 250 mg tablet
On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP 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
- Proficient Rx LP, Thousand Oaks, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Terbinafine: every company that makes it
- Form
- tablet, oral
- Strength
- 250 mg
- Approval
- ANDA ANDA078297
- On the market since
- Jul 2, 2007
- Package NDCs
71205-061-3071205-061-35- Official label
- DailyMed (National Library of Medicine), updated Sep 1, 2024
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