NDC 72789-156
Cyclobenzaprine Hydrochloride 10 mg tablet, film coated
On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. 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
- 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, oral
- Strength
- 10 mg
- Approval
- ANDA ANDA077797
- On the market since
- Mar 30, 2017
- Package NDCs
72789-156-15- Official label
- DailyMed (National Library of Medicine), updated Oct 15, 2026
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