# Guaifenesin and Dextromethorphan HBR

NDC: 43598-231
Generic name: Guaifenesin and Dextromethorphan HBR
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: 20230815

FDA application: ANDA217340

## Active ingredients

- DEXTROMETHORPHAN HYDROBROMIDE: 30 mg/1
- GUAIFENESIN: 600 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43598-231"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43598-231
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5e95d8c0-d521-45b6-ccaf-7786fbd14d5c