# CYPROHEPTADINE HYDROCHLORIDE

NDC: 70752-232
Generic name: CYPROHEPTADINE HYDROCHLORIDE
Labeler / Manufacturer: Quagen Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20261015

FDA application: ANDA212491

## Active ingredients

- CYPROHEPTADINE HYDROCHLORIDE: 2 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70752-232"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70752-232