# Guaifenesin Extended-Release 600 mg

NDC: 53041-233
Generic name: Guaifenesin
Labeler / Manufacturer: Guardian Drug Company
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20180301

FDA application: ANDA209215

## Active ingredients

- GUAIFENESIN: 600 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"53041-233"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=53041-233
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=20f9e083-419d-429d-a570-24b312ed5d2a