# GUAIFENESIN

NDC: 82804-265
Generic name: GUAIFENESIN
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20220819

FDA application: ANDA213420

## Active ingredients

- GUAIFENESIN: 600 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"82804-265"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=82804-265
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=28b31f37-6896-40f5-8f3a-60c93c5c1278