# Fluoxetine

NDC: 84386-106
Generic name: Fluoxetine
Labeler / Manufacturer: Aurobindo Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20260115

FDA application: ANDA213265

## Active ingredients

- FLUOXETINE HYDROCHLORIDE: 60 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"84386-106"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=84386-106
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a9ed97dd-8041-4a02-889c-dcb8b2805f36