# Dextromethorphan hydrobromide and quinidine sulfate

NDC: 31722-693
Generic name: Dextromethorphan hydrobromide and quinidine sulfate
Labeler / Manufacturer: Camber Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20240828

FDA application: ANDA218426

## 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:"31722-693"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=31722-693
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7028dcb7-f436-4cf6-9beb-23c1d215c798