# Mucinex

NDC: 68084-572
Generic name: Guaifenesin
Labeler / Manufacturer: American Health Packaging
Product type: HUMAN OTC DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20160219

FDA application: NDA021282

## 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:"68084-572"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68084-572
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0129f47d-abc2-414c-b4e1-1064c5d6a623