# GUAIFENESIN

NDC: 68196-960
Generic name: GUAIFENESIN
Labeler / Manufacturer: Sam's West Inc
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20250731

FDA application: ANDA210453

## 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:"68196-960"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68196-960
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3867a132-1a87-5e08-e063-6294a90a6dc8