# Dextromethorphan Hydrobromide and Quinidine Sulphate

NDC: 63304-650
Generic name: Dextromethorphan Hydrobromide and Quinidine Sulphate
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20260730

FDA application: ANDA204196

## Active ingredients

- DEXTROMETHORPHAN HYDROBROMIDE: 20 mg/1
- QUINIDINE SULFATE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63304-650"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63304-650
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=92b54ac4-594e-47b8-a4d3-394a29b425f3