# Cyproheptadine Hydrochloride

NDC: 64980-504
Generic name: Cyproheptadine Hydrochloride
Labeler / Manufacturer: Rising Pharma Holdings, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SYRUP
Routes: ORAL
Marketing started: 20060710

FDA application: ANDA040668

## Active ingredients

- CYPROHEPTADINE HYDROCHLORIDE: 2 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"64980-504"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=64980-504
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e2bf4d46-6585-41d9-868c-98603b165d5b