# Fluvoxamine maleate

NDC: 0832-1672
Generic name: Fluvoxamine maleate
Labeler / Manufacturer: Upsher-Smith Laboratories, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20001129
Marketing ended: 20260630
FDA application: ANDA075888

## Active ingredients

- FLUVOXAMINE MALEATE: 100 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0832-1672"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0832-1672
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=52b29024-b639-4c88-ac6c-0c64dbd204f4
