NDC 53149-4852
Cyclobenzaprine Hydrochloride 7.5 mg tablet, film coated
On the label: All Pharma, LLC. It's repackaged from NDC 71085-010, made by Ipg Pharmaceuticals, Inc. (Cyclobenzaprine Hydrochloride). That product's FDA listing has since ended, so its label and factories are no longer published.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| All Pharma, LLC | Miami Lakes, Florida, United States | Makes it and repackages it | Problems found, fixed voluntarilyDec 22, 2021 · 2 inspections |
Product details
- Generic drug
- Cyclobenzaprine: every company that makes it
- Form
- tablet, film coated
- Strength
- 7.5 mg
- Approval
- ANDA ANDA078722
- On the market since
- Aug 1, 2017
- Package NDCs
53149-4852-153149-4852-353149-4852-653149-4852-9- Official label
- DailyMed (National Library of Medicine), updated Aug 13, 2018
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