# Fexofenadine hydrochloride

NDC: 68001-439
Generic name: Fexofenadine hydrochloride
Labeler / Manufacturer: BluePoint Laboratories
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20200619

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:"68001-439"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68001-439
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a86aebd0-937e-5d73-e053-2995a90a656a