# Cyproheptadine Hydrochloride

NDC: 39328-544
Generic name: Cyproheptadine Hydrochloride
Labeler / Manufacturer: Patrin Pharma, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20220215

FDA application: ANDA209108

## Active ingredients

- CYPROHEPTADINE: 2 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"39328-544"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=39328-544
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=81d9523f-f945-4410-8b71-8b5fea48a3da