# Fluoxetine

NDC: 62332-243
Generic name: Fluoxetine
Labeler / Manufacturer: Alembic Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20170407

FDA application: ANDA208698

## Active ingredients

- FLUOXETINE HYDROCHLORIDE: 20 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"62332-243"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62332-243
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e9ee6e93-4a57-4fd1-a417-3944484dd32c