# cyproheptadine hydrochloride solution

NDC: 58657-697
Generic name: CYPROHEPTADINE HYDROCHLORIDE
Labeler / Manufacturer: Method Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20240615

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:"58657-697"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=58657-697
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1acfd050-6c07-a269-e063-6394a90a77e8