# fluoxetine hydrochloride

NDC: 72162-1495
Generic name: fluoxetine hydrochloride
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20160822

FDA application: ANDA203836

## Active ingredients

- FLUOXETINE HYDROCHLORIDE: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72162-1495"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72162-1495
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a04a5bed-d051-4bb4-ae20-b09b10d5c181