# Atomoxetine Hydrochloride

NDC: 60505-2831
Generic name: atomoxetine hydrochloride
Labeler / Manufacturer: Apotex Corp.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20180521

FDA application: ANDA078983

## Active ingredients

- ATOMOXETINE HYDROCHLORIDE: 18 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60505-2831"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60505-2831
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=132852a6-5bff-15dd-255c-98309dd83630