# Quetiapine fumarate

NDC: 47335-902
Generic name: Quetiapine fumarate
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20120328

FDA application: ANDA201190

## Active ingredients

- QUETIAPINE FUMARATE: 25 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"47335-902"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=47335-902
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ffe52b98-9872-48c1-90fd-8fcd37c3432f