# Fexofenadine HCl and Pseudoephedrine HCI

NDC: 43598-823
Generic name: Fexofenadine HCl and Pseudoephedrine HCI
Labeler / Manufacturer: Dr. Reddy's Laboratories Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20190718

FDA application: ANDA076667

## 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:"43598-823"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43598-823
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6fd05737-d996-b5b6-dccf-bc179a9d606c