# Guaifenesin and Pseudoephedrine HCl

NDC: 46122-801
Generic name: Guaifenesin and Pseudoephedrine HCl
Labeler / Manufacturer: Amerisource Bergen
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20241001

FDA application: ANDA213203

## Active ingredients

- GUAIFENESIN: 600 mg/1
- PSEUDOEPHEDRINE HYDROCHLORIDE: 60 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"46122-801"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=46122-801
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=775000bc-56de-4c72-87da-65bb33f063b3