# mucus relief

NDC: 41250-654
Generic name: guaifenesin
Labeler / Manufacturer: Meijer Distribution Inc
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, MULTILAYER, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20210223
Marketing ended: 20261001
FDA application: ANDA213420

## 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:"41250-654"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=41250-654
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a0510998-d297-4222-857c-c8e80c657ddf