NDC 71335-2264
Cevimeline Hydrochloride 30 mg capsule
On the label: Bryant Ranch Prepack. It's repackaged: Bryant Ranch Prepack rebottles it from Hikma Pharmaceuticals USA Inc.'s NDC 0054-0334.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| West-Ward Columbus Inc. | Columbus, OH, United States | Makes it | No problems foundApr 30, 2026 · 27 inspections |
Repackaging site
- Bryant Ranch Prepack, Burbank, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Cevimeline: every company that makes it
- Form
- capsule, oral
- Strength
- 30 mg
- Approval
- ANDA ANDA091591
- On the market since
- Jul 8, 2013
- Package NDCs
71335-2264-171335-2264-271335-2264-3- Official label
- DailyMed (National Library of Medicine), updated Oct 8, 2024
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