# Fexofenadine Hydrochloride

NDC: 45802-847
Generic name: fexofenadine hydrochloride
Labeler / Manufacturer: Padagis Israel Pharmaceuticals Ltd
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20220107

FDA application: ANDA212971

## 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:"45802-847"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=45802-847
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e43b561e-d68a-47af-be93-d710f0f77505