# Cyproheptadine Hydrochloride

NDC: 52817-210
Generic name: Cyproheptadine Hydrochloride
Labeler / Manufacturer: TRUPHARMA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20170117

FDA application: ANDA206553

## Active ingredients

- CYPROHEPTADINE HYDROCHLORIDE: 4 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"52817-210"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=52817-210
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9c0b47c0-ecd2-450f-9dcb-c262db92866e