# Mucus Relief Extended Release Maximum Strength

NDC: 0363-0832
Generic name: Guaifenesin
Labeler / Manufacturer: Walgreens
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20180831
Marketing ended: 20261231
FDA application: ANDA207342

## 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:"0363-0832"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0363-0832
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e4b27b9b-5f3b-4314-9717-54d73cf6b74e