NDC 72789-102
Cyproheptadine Hydrochloride 4 mg tablet
On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. rebottles it from Unichem Pharmaceuticals (USA), Inc.'s NDC 76385-130.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Beximco Pharmaceuticals PLC | Tongi, Bangladesh | Makes it | Problems found, fixed voluntarilyMar 30, 2023 · 2 inspections |
Repackaging site
- PD-Rx Pharmaceuticals Inc., Oklahoma City, OK, United States · repackages it
Product details
- Generic drug
- Cyproheptadine: every company that makes it
- Form
- tablet, oral
- Strength
- 4 mg
- Approval
- ANDA ANDA206676
- On the market since
- Mar 1, 2020
- Package NDCs
72789-102-0172789-102-30- Official label
- DailyMed (National Library of Medicine), updated Feb 16, 2026
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