# Fexofenadine HCL

NDC: 16714-899
Generic name: Fexofenadine HCL
Labeler / Manufacturer: NorthStar RxLLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20190218

FDA application: ANDA204097

## 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:"16714-899"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=16714-899
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9c308a91-640d-441b-8fb5-acb5a415405e