# Atomoxetine

NDC: 55111-522
Generic name: Atomoxetine
Labeler / Manufacturer: Dr. Reddy's Laboratories Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20180223

FDA application: ANDA090609

## 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:"55111-522"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55111-522
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=973bdc9b-6421-7e00-e2b6-3cce036d363e