# Naratriptan

NDC: 0054-0278
Generic name: Naratriptan
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20100707

FDA application: ANDA090381

## Active ingredients

- NARATRIPTAN HYDROCHLORIDE: 1 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0054-0278"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0054-0278
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fd1944b3-8054-4faa-a82e-d818dfdd3875