# fluoxetine

NDC: 75834-148
Generic name: fluoxetine hydrochloride
Labeler / Manufacturer: NIVAGEN PHARMACEUTICALS, INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20171211

FDA application: ANDA209695

## Active ingredients

- FLUOXETINE HYDROCHLORIDE: 60 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"75834-148"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=75834-148
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f4cbf9a9-1d7f-4aa0-a18d-fba50d49bd2b