# atomoxetine

NDC: 50090-7463
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: 20170530

FDA application: ANDA079019

## Active ingredients

- ATOMOXETINE HYDROCHLORIDE: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50090-7463"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50090-7463
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=90f45a1e-f79f-468f-b21b-5dc82f5717aa