# Guaifenesin

NDC: 51660-566
Generic name: Guaifenesin
Labeler / Manufacturer: Ohm Laboratories, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20220401

FDA application: ANDA209254

## 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:"51660-566"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51660-566
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7076e42a-17ff-4c42-9963-2dc02c0a5e49