# GUAIFENESIN

NDC: 80513-413
Generic name: GUAIFENESIN
Labeler / Manufacturer: Advanced Rx LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20201218

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:"80513-413"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=80513-413
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cb7cd1df-8cfb-4a9c-9567-809a2343622e