# Mucus Relief Extended Release Maximum Strength

NDC: 37808-762
Generic name: Guaifenesin
Labeler / Manufacturer: H E B
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20210802

FDA application: ANDA207342

## Active ingredients

- GUAIFENESIN: 1200 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"37808-762"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=37808-762
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6f075c29-8256-4cac-96c4-a772a53ad21d