NDC 53808-0829
Cyproheptadine Hydrochloride 4 mg tablet
On the label: State of Florida DOH Central Pharmacy. It's repackaged from NDC 0093-2929, made by Teva Pharmaceuticals USA, Inc. (Cyproheptadine Hydrochloride). That product's FDA listing has since ended, so its label and factories are no longer published.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| State of Florida DOH Central Pharmacy | Location not on file | Makes it | Not inspected on record |
Product details
- Generic drug
- Cyproheptadine: every company that makes it
- Form
- tablet
- Strength
- 4 mg
- Approval
- ANDA ANDA087056
- On the market since
- Jan 1, 2013
- Package NDCs
53808-0829-1- Official label
- DailyMed (National Library of Medicine), updated Sep 9, 2013
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