NDC 87063-180
Cevimeline Hydrochloride 30 mg capsule
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Rising Pharma Holdings, Inc.'s NDC 16571-657.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Ingenus Pharmaceuticals NJ, LLC | Fairfield, NJ, United States | Makes it | No problems foundJan 9, 2026 · 11 inspections |
Repackaging site
- Asclemed USA Inc. dba Enovachem, Torrance, 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 ANDA203775
- On the market since
- Jun 17, 2014
- Package NDCs
87063-180-0187063-180-3087063-180-6087063-180-90- Official label
- DailyMed (National Library of Medicine), updated May 18, 2026
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