# Fexofenadine hydrochloride

NDC: 43598-809
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: 20181226

FDA application: ANDA076502

## Active ingredients

- FEXOFENADINE HYDROCHLORIDE: 180 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43598-809"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43598-809
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=624b3a91-af4f-8848-6fc3-392e0df34cc8