NDC 82804-220
terbinafine hydrochloride 250 mg tablet
On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP rebottles it from Bionpharma Inc.'s NDC 69452-351.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| OrBion Pharmaceuticals Private Limited | Kancheepuram, India | Makes it, tests it, packages it and labels it | No problems foundOct 27, 2025 · 6 inspections |
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 ANDA078163
- On the market since
- Jan 28, 2022
- Package NDCs
82804-220-3082804-220-42- Official label
- DailyMed (National Library of Medicine), updated Sep 1, 2025
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