# Fluoxetine hydrochloride

NDC: 43598-632
Generic name: Fluoxetine hydrochloride
Labeler / Manufacturer: Dr. Reddy's Laboratories Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20190128

FDA application: ANDA211721

## 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:"43598-632"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43598-632
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=80e52273-9741-6aef-eb24-8a93ead85ba7