# Allergy Relief

NDC: 63868-334
Generic name: Fexofenadine Hydrochloride
Labeler / Manufacturer: CHAIN DRUG MARKETING ASSOCIATION INC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20210706

FDA application: ANDA211075

## 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:"63868-334"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63868-334
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c5d58d74-da08-eb72-e053-2a95a90adc27