# Mucinex DM

NDC: 85237-1650
Generic name: Guaifenesin and Dextromethorphan Hydrobromide
Labeler / Manufacturer: Select Consumer Group
Product type: HUMAN OTC DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20120626

FDA application: NDA021620

## Active ingredients

- DEXTROMETHORPHAN HYDROBROMIDE: 30 mg/1
- GUAIFENESIN: 600 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"85237-1650"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=85237-1650
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3c9c8fb0-8a00-4b0f-e063-6394a90af632