NDC 70518-3517
Cyproheptadine Hydrochloride 4 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack 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 |
Product details
- Generic drug
- Cyproheptadine: every company that makes it
- Form
- tablet, oral
- Strength
- 4 mg
- Approval
- ANDA ANDA212491
- On the market since
- Sep 13, 2022
- Package NDCs
70518-3517-0- Official label
- DailyMed (National Library of Medicine), updated Apr 10, 2026
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