# Fexofenadine Hydrochloride

NDC: 43598-936
Generic name: Fexofenadine hydrochloride
Labeler / Manufacturer: Dr. Reddy's Laboratories Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20201201

FDA application: ANDA076502

## Active ingredients

- FEXOFENADINE HYDROCHLORIDE: 60 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43598-936"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43598-936
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b0121213-eae1-8429-9986-3b3b26f35e47