# ATONCY

NDC: 30698-456
Generic name: Atomoxetine hydrochloride
Labeler / Manufacturer: Validus Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20260320

FDA application: NDA220320

## Active ingredients

- ATOMOXETINE HYDROCHLORIDE: 4 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"30698-456"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=30698-456
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=72d3d8cf-7f3b-479e-bd9f-e204d4118517