# UP AND UP MUCUS RELIEF

NDC: 82442-503
Generic name: guaifenesin
Labeler / Manufacturer: Target Corporation
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, MULTILAYER, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20250917

FDA application: ANDA078912

## 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:"82442-503"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=82442-503
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=059cff23-b6a5-40dc-ac4e-9bcb552e9764