# Guaifenesin 1200 mg

NDC: 43598-009
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: 20220315

FDA application: ANDA215932

## 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:"43598-009"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43598-009
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=99307c61-5df3-0a83-1e21-ddb03bc905b4