# Cyproheptadine Hydrochloride

NDC: 62135-236
Generic name: Cyproheptadine Hydrochloride
Labeler / Manufacturer: Chartwell RX, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 19830526

FDA application: ANDA088212

## 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:"62135-236"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62135-236
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=029ed3b6-175e-4a1a-81ed-350bff5f6167