NDC 76420-896
Cyclobenzaprine Hydrochloride 30 mg capsule, extended release
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Upsher-Smith Laboratories, Inc.'s NDC 24979-036.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Bora Pharmaceutical Laboratories Inc. Zhongli Plant | Taoyuan City, Taiwan | Makes it, tests it and packages it | Problems found, fixed voluntarilyFeb 7, 2020 · 4 inspections |
| Bora Pharmaceutical Laboratories Inc. Zhongli Plant Building II | Taoyuan City, Taiwan | Makes it, tests it and packages it | Problems found, fixed voluntarilyFeb 7, 2020 · 4 inspections |
| Bora Pharmaceutical Laboratories Inc. | Zhunan Township, Taiwan | Packages it | Problems found, fixed voluntarilyJul 21, 2025 · 7 inspections |
Repackaging site
- Asclemed USA Inc. dba Enovachem, Torrance, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Cyclobenzaprine: every company that makes it
- Form
- capsule, extended release, oral
- Strength
- 30 mg
- Approval
- ANDA ANDA091281
- On the market since
- Mar 1, 2019
- Package NDCs
76420-896-0176420-896-3076420-896-6076420-896-90- Official label
- DailyMed (National Library of Medicine), updated Jan 7, 2025
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