NDC 72789-457
Cevimeline Hydrochloride 30 mg capsule
On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. rebottles it from Advagen Pharma Ltd.'s NDC 72888-118.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Rubicon Research Limited | Thane, India | Makes it, tests it and labels it | No problems foundMar 8, 2024 · 5 inspections |
Repackaging site
- PD-Rx Pharmaceuticals Inc., Oklahoma City, OK, United States · repackages it
Product details
- Generic drug
- Cevimeline: every company that makes it
- Form
- capsule, oral
- Strength
- 30 mg
- Approval
- ANDA ANDA216682
- On the market since
- Apr 6, 2023
- Package NDCs
72789-457-0172789-457-30- Official label
- DailyMed (National Library of Medicine), updated Aug 27, 2026
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