# Guaifenesin

NDC: 69848-018
Generic name: Guaifenesin
Labeler / Manufacturer: GRANULES USA, INC.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20240912

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:"69848-018"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69848-018
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a62e2045-8ec2-1771-e053-2995a90a03b4