# Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride

NDC: 58602-807
Generic name: Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride
Labeler / Manufacturer: Aurohealth LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20171030

FDA application: ANDA209116

## Active ingredients

- FEXOFENADINE HYDROCHLORIDE: 60 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:"58602-807"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=58602-807
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4726af84-83c1-456d-995c-f6a8d1583f8b