# Mucus Relief

NDC: 37808-935
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: 20210528

FDA application: ANDA207342

## Active ingredients

- GUAIFENESIN: 600 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"37808-935"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=37808-935
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=562b6ab6-4795-4909-8008-e919173844c9