# Fluoxetine

NDC: 62332-024
Generic name: Fluoxetine
Labeler / Manufacturer: Alembic Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20160129

FDA application: ANDA090223

## Active ingredients

- FLUOXETINE HYDROCHLORIDE: 40 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"62332-024"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62332-024
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9de65da4-73f8-4c88-8198-c92e63224ddb