# Guaifenesin 600 mg

NDC: 25000-042
Generic name: Guaifenesin 600 mg
Labeler / Manufacturer: MARKSANS PHARMA LIMITED
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20230823

FDA application: ANDA217780

## 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:"25000-042"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=25000-042
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fedf43d0-d6d1-4f50-bbab-396701e45cb2