NDC 70710-1110
Cyproheptadine Hydrochloride 4 mg tablet
On the label: Zydus Pharmaceuticals (USA) Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zydus Lifesciences Limited | Ahmedabad, India | Makes it and tests it | Problems found, fixed voluntarilyMar 24, 2023 · 5 inspections |
Product details
- Generic drug
- Cyproheptadine: every company that makes it
- Form
- tablet, oral
- Strength
- 4 mg
- Approval
- ANDA ANDA208938
- On the market since
- Jul 20, 2017
- Package NDCs
70710-1110-070710-1110-1- Official label
- DailyMed (National Library of Medicine), updated Oct 4, 2022
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