# FLUOXETINE

NDC: 68788-8618
Generic name: FLUOXETINE
Labeler / Manufacturer: Preferred Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20240328

FDA application: ANDA201336

## Active ingredients

- FLUOXETINE HYDROCHLORIDE: 40 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68788-8618"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68788-8618
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=54ded68c-1d2e-453d-b155-84c3102e1f0e