# FLUOXETINE

NDC: 23155-030
Generic name: FLUOXETINE
Labeler / Manufacturer: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20241013

FDA application: ANDA201336

## Active ingredients

- FLUOXETINE HYDROCHLORIDE: 40 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"23155-030"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=23155-030
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6f4e4e9f-9ded-452f-b3ef-ab6aa9c72952