# MUCUS RELIEF GUAIFENESIN EXTENDED-RELEASE 600 mg

NDC: 73581-401
Generic name: GUAIFENESIN
Labeler / Manufacturer: YYBA CORP
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20220302

FDA application: ANDA213420

## 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:"73581-401"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=73581-401
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d9d1ce2d-d96a-4950-e053-2995a90ad988