# Mucus Relief DM

NDC: 37808-834
Generic name: Guaifenesin, Dextromethorphan HBr
Labeler / Manufacturer: H E B
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20230315

FDA application: ANDA209692

## Active ingredients

- DEXTROMETHORPHAN HYDROBROMIDE: 60 mg/1
- GUAIFENESIN: 1200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"37808-834"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=37808-834
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=20df2ffe-5281-4cd6-adb3-3a3d28788ef6