NDC 42708-177
Cyproheptadine Hydrochloride 4 mg tablet
On the label: QPharma, Inc.. It's repackaged: QPharma, Inc. rebottles it from TruPharma LLC.'s NDC 52817-210.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Piramal Pharma Limited | Pithampur, India | Makes it, tests it and packages it | No problems foundMay 19, 2023 · 8 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 ANDA206553
- On the market since
- Jan 17, 2017
- Package NDCs
42708-177-21- Official label
- DailyMed (National Library of Medicine), updated Dec 2, 2025
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