# Atomoxetine

NDC: 50090-6127
Generic name: Atomoxetine
Labeler / Manufacturer: A-S Medication Solutions
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20210311

FDA application: ANDA202682

## Active ingredients

- ATOMOXETINE HYDROCHLORIDE: 80 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50090-6127"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50090-6127
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=652cb30f-4368-4009-93a3-3a0d2a365f42