NDC 42708-197
Cyclobenzaprine Hydrochloride 5 mg tablet, film coated
On the label: QPharma, Inc.. It's repackaged: QPharma, Inc. rebottles it from TruPharma LLC.'s NDC 52817-330.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants TruPharma LLC. names for other drugs.
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 ANDA208170
- On the market since
- May 31, 2017
- Package NDCs
42708-197-20- Official label
- DailyMed (National Library of Medicine), updated Apr 10, 2026
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