NDC 42708-172
Cyclobenzaprine Hydrochloride 5 mg tablet, film coated
On the label: QPharma, Inc.. It's repackaged: QPharma, Inc. rebottles it from Rising Pharma Holdings, Inc.'s NDC 16571-782.
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
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Product details
- Generic drug
- Cyclobenzaprine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 5 mg
- Approval
- ANDA ANDA078643
- On the market since
- Sep 26, 2008
- Package NDCs
42708-172-20- Official label
- DailyMed (National Library of Medicine), updated Dec 2, 2025
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