# fexofenadine hcl

NDC: 50228-201
Generic name: fexofenadine hcl
Labeler / Manufacturer: ScieGen Pharmaceuticals, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20141226

FDA application: ANDA204507

## Active ingredients

- FEXOFENADINE HYDROCHLORIDE: 60 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50228-201"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50228-201
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b7e9477d-33d9-4463-b8a6-69af5f71ce35