NDC 42708-187
Cyproheptadine Hydrochloride 4 mg tablet
On the label: QPharma, Inc.. It's repackaged: QPharma, Inc. rebottles it from Quagen Pharmaceuticals LLC's NDC 70752-107.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Quagen Pharmaceuticals LLC | West Caldwell, NJ, United States | Makes it and packages it | No problems foundApr 17, 2026 · 3 inspections |
Repackaging site
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Product details
- Generic drug
- Cyproheptadine: every company that makes it
- Form
- tablet, oral
- Strength
- 4 mg
- Approval
- ANDA ANDA212491
- On the market since
- Feb 24, 2021
- Package NDCs
42708-187-21- Official label
- DailyMed (National Library of Medicine), updated Dec 1, 2025
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