# Quetiapine

NDC: 71335-2641
Generic name: Quetiapine
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20220815

FDA application: ANDA215478

## Active ingredients

- QUETIAPINE FUMARATE: 400 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71335-2641"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71335-2641
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a373a57d-1dee-4bd1-b71b-494e1662f558