# Fluoxetine

NDC: 65862-192
Generic name: Fluoxetine Hydrochloride
Labeler / Manufacturer: Aurobindo Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20080131
Marketing ended: 20280229
FDA application: ANDA078619

## Active ingredients

- FLUOXETINE HYDROCHLORIDE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65862-192"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65862-192
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=45454555-7402-41cb-a452-e6a76e04f387