# Mucus Relief Extended Release

NDC: 11673-732
Generic name: Guaifenesin
Labeler / Manufacturer: TARGET Corporation
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20180711

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:"11673-732"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=11673-732
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e521e8e1-8227-451a-8858-01c26f6e0657