NDC 70518-3474
Cyclobenzaprine Hydrochloride 10 mg tablet, film coated
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Rising Pharma Holdings, Inc.'s NDC 16571-783.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Medchal, India | Makes it and tests it | Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action |
Product details
- Generic drug
- Cyclobenzaprine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 10 mg
- Approval
- ANDA ANDA078643
- On the market since
- Aug 9, 2022
- Package NDCs
70518-3474-070518-3474-170518-3474-270518-3474-370518-3474-470518-3474-570518-3474-670518-3474-770518-3474-870518-3474-9- Official label
- DailyMed (National Library of Medicine), updated Aug 10, 2026
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