# Guaifenesin and Dextromethorphan HBr

NDC: 51660-301
Generic name: Guaifenesin and Dextromethorphan HBr
Labeler / Manufacturer: OHM LABORATORIES 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: 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:"51660-301"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51660-301
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f2eb5494-2672-444f-afa3-d1ef8ed1eaa1