# Allergy Relief non drowsy

NDC: 41250-506
Generic name: Fexofenadine HCl
Labeler / Manufacturer: MEIJER, INC.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20180331
Marketing ended: 20261231
FDA application: ANDA204507

## 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:"41250-506"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=41250-506
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b3395454-65db-4d8b-abce-2475b049a114