# ALLEGRA-D

NDC: 50090-1203
Generic name: fexofenadine hydrochloride and pseudoephedrine hydrochloride
Labeler / Manufacturer: A-S Medication Solutions
Product type: HUMAN OTC DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20110303

FDA application: NDA020786

## Active ingredients

- FEXOFENADINE HYDROCHLORIDE: 60 mg/1
- PSEUDOEPHEDRINE HYDROCHLORIDE: 120 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50090-1203"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50090-1203
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=705e1087-61cb-43c3-8675-f56626a1707b