NDC 51655-063
Tadalafil 20 mg tablet, film coated
On the label: Northwind Pharmaceuticals. It's repackaged: Northwind Pharmaceuticals rebottles it from Zydus Pharmaceuticals (USA) Inc.'s NDC 68382-899.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zydus Lifesciences Limited | Ahmedabad, India | Makes it and tests it | Problems found, fixed voluntarilyAug 5, 2022 · 10 inspections, 3 with FDA action |
Repackaging site
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Product details
- Generic drug
- Tadalafil: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA206693
- On the market since
- Sep 27, 2022
- Package NDCs
51655-063-5451655-063-87- Official label
- DailyMed (National Library of Medicine), updated Dec 26, 2025
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