# Fexofenadine hydrochloride

NDC: 0904-6711
Generic name: Fexofenadine hydrochloride
Labeler / Manufacturer: MAJOR PHARMACEUTICALS
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20180427
Marketing ended: 20260831
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:"0904-6711"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0904-6711
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0a6da401-a8a3-5d0b-f37e-c220838f7e49