# Quetiapine

NDC: 0093-8162
Generic name: Quetiapine
Labeler / Manufacturer: Teva Pharmaceuticals USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20120327

FDA application: ANDA077745

## Active ingredients

- QUETIAPINE FUMARATE: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0093-8162"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0093-8162
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c1d4ef59-bf58-44fe-9b46-1af42e2f7f8b