# Atomoxetine Hydrochloride

NDC: 51407-101
Generic name: atomoxetine hydrochloride
Labeler / Manufacturer: Golden State Medical Supply, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20170530

FDA application: ANDA078983

## Active ingredients

- ATOMOXETINE HYDROCHLORIDE: 18 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51407-101"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51407-101
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6f14ced9-c16c-905a-e053-2a91aa0a031e