NDC 70934-063
Cyclobenzaprine Hydrochloride 10 mg tablet, film coated
On the label: Denton Pharma, Inc. DBA Northwind Pharmaceuticals.. It's repackaged: Denton Pharma, Inc. DBA Northwind Pharmaceuticals. rebottles it from Solco Healthcare U.S., LLC's NDC 43547-400.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Generics Bidco II LLC d/b/a Prinston Laboratories | Charlotte, NC, United States | Makes it | Problems found, fixed voluntarilySep 19, 2025 · 10 inspections, 1 with FDA action |
Repackaging site
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals, Location not on file · repackages it
Product details
- Generic drug
- Cyclobenzaprine: every company that makes it
- Form
- tablet, film coated
- Strength
- 10 mg
- Approval
- ANDA ANDA077797
- On the market since
- Jan 15, 2018
- Package NDCs
70934-063-1570934-063-2070934-063-30- Official label
- DailyMed (National Library of Medicine), updated Jan 11, 2021
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