# Guaifenesin 600 mg

NDC: 43598-110
Generic name: Guaifenesin
Labeler / Manufacturer: Dr. Reddy's Laboratories Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20220901

FDA application: ANDA215932

## 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:"43598-110"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43598-110
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=525fda90-134c-f038-c403-eb5ffc1fb1f1