# Fluoxetine

NDC: 77771-113
Generic name: Fluoxetine Hydrochloride
Labeler / Manufacturer: RADHA PHARMACEUTICALS, INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20221024

FDA application: ANDA204597

## Active ingredients

- FLUOXETINE HYDROCHLORIDE: 10 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"77771-113"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=77771-113
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1a07ebe9-3661-4a48-b8af-9b228875166a