NDC 43063-516
Cyclobenzaprine Hydrochloride 10 mg tablet, film coated
On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. rebottles it from KVK-TECH, Inc.'s NDC 10702-007.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Kvk-Tech, Inc. | Newtown, PA, United States | Makes it | Serious problems, FDA actionMar 14, 2025 · 13 inspections, 3 with FDA action |
Repackaging site
- PD-Rx Pharmaceuticals Inc., Oklahoma City, OK, United States · repackages it
Product details
- Generic drug
- Cyclobenzaprine: every company that makes it
- Form
- tablet, film coated
- Strength
- 10 mg
- Approval
- ANDA ANDA078048
- On the market since
- Jul 31, 2014
- Package NDCs
43063-516-0143063-516-0343063-516-0443063-516-0643063-516-0943063-516-1043063-516-1243063-516-1443063-516-1543063-516-2043063-516-2143063-516-30- Official label
- DailyMed (National Library of Medicine), updated Oct 11, 2024
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