# Atomoxetine

NDC: 31722-720
Generic name: Atomoxetine
Labeler / Manufacturer: Camber Pharmaceuticals, Inc.
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: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"31722-720"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=31722-720
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f266ab7b-5a68-42b5-b204-e3249bea0aed