# Nuedexta

NDC: 59148-053
Generic name: dextromethorphan hydrobromide and quinidine sulfate
Labeler / Manufacturer: Otsuka America Pharmaceutical, Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: CAPSULE, GELATIN COATED
Routes: ORAL
Marketing started: 20230103

FDA application: NDA021879

## 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:"59148-053"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=59148-053
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c8cce784-8c5f-415b-8068-76e5d481d159