# ATOMOXETINE

NDC: 82619-119
Generic name: atomoxetine
Labeler / Manufacturer: Creekwood Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20260706

FDA application: ANDA218875

## Active ingredients

- ATOMOXETINE HYDROCHLORIDE: 60 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"82619-119"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=82619-119
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9b757805-eabf-4301-85be-7a3e38f6b187