# QUETIAPINE

NDC: 70518-4699
Generic name: QUETIAPINE
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20260715

FDA application: ANDA204253

## Active ingredients

- QUETIAPINE FUMARATE: 200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-4699"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-4699
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=67872105-4ec6-4d46-b3b4-c672c93576d2