# Guaifenesin and Dextromethorphan HBr

NDC: 63304-110
Generic name: Guaifenesin and Dextromethorphan HBr
Labeler / Manufacturer: SUN PHARMACEUTICAL INDUSTRIES, INC.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20210701

FDA application: ANDA214781

## Active ingredients

- DEXTROMETHORPHAN HYDROBROMIDE: 60 mg/1
- GUAIFENESIN: 1200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63304-110"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63304-110
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=06328741-03e3-49cf-ae44-d4c2116e38a3