# Guaifenesin

NDC: 71179-002
Generic name: Guaifenesin
Labeler / Manufacturer: VESPYR BRANDS LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20220627

FDA application: ANDA210453

## Active ingredients

- GUAIFENESIN: 1200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71179-002"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71179-002
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e2e3c628-d241-42b6-8c1e-ef997ffa6e87