# Atomoxetine

NDC: 0093-3545
Generic name: Atomoxetine
Labeler / Manufacturer: Teva Pharmaceuticals USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20170530

FDA application: ANDA079022

## 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:"0093-3545"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0093-3545
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4953df7b-ccdb-452c-8699-5fd7259609b4