# CYPROHEPTADINE HYDROCHLORIDE

NDC: 70710-1110
Generic name: CYPROHEPTADINE HYDROCHLORIDE
Labeler / Manufacturer: Zydus Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20170720

FDA application: ANDA208938

## 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:"70710-1110"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70710-1110
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=766f9b59-2c72-45ac-af09-5dd6c3e16b52