# Maximum Strength Mucus Relief

NDC: 68196-033
Generic name: Guaifenesin
Labeler / Manufacturer: SAM'S WEST INC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20250820

FDA application: ANDA217780

## 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:"68196-033"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68196-033
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=39282544-e1e8-8270-e063-6394a90a23fe