# Atomoxetine

NDC: 71335-2162
Generic name: Atomoxetine
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20170530

FDA application: ANDA079016

## Active ingredients

- ATOMOXETINE HYDROCHLORIDE: 40 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71335-2162"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71335-2162
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d4fe9217-1853-4f8b-9a93-77e511554ca1