# Naratriptan

NDC: 69452-341
Generic name: Naratriptan
Labeler / Manufacturer: Bionpharma Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20220411

FDA application: ANDA091441

## Active ingredients

- NARATRIPTAN HYDROCHLORIDE: 2.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69452-341"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69452-341
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=93b7e6c2-e6a7-4f6b-9ecd-62d6bb0a6dda