# Guaifenesin and Pseudoephedrine HCL

NDC: 55111-799
Generic name: Guaifenesin and Pseudoephedrine HCL
Labeler / Manufacturer: Dr. Reddys Laboratories Limited
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20171229

FDA application: ANDA208369

## Active ingredients

- GUAIFENESIN: 1200 mg/1
- PSEUDOEPHEDRINE HYDROCHLORIDE: 120 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"55111-799"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55111-799
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=845a2dcc-9069-3141-ae13-f2063f36d130