# CYPROHEPTADINE HYDROCHLORIDE

NDC: 50742-190
Generic name: CYPROHEPTADINE HYDROCHLORIDE
Labeler / Manufacturer: Ingenus Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20150923

FDA application: ANDA205087

## 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:"50742-190"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50742-190
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=56f428c9-8d33-4c91-91d8-1fe194335066