# Mucus Relief Extended Release Maximum Strength

NDC: 69256-732
Generic name: Guaifenesin
Labeler / Manufacturer: Harris Teeter, LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20210528
Marketing ended: 20260528
FDA application: ANDA207342

## Active ingredients

- GUAIFENESIN: 1200 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69256-732"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69256-732
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e1ca82fe-224f-4cdd-9992-2754c1e508e1