# Fexofenadine HCl and Pseudoephedrine HCl

NDC: 43598-892
Generic name: Fexofenadine HCl and Pseudoephedrine HCl
Labeler / Manufacturer: Dr.Reddy's Laboratories Inc
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20220517
Marketing ended: 20260831
FDA application: ANDA079043

## Active ingredients

- FEXOFENADINE HYDROCHLORIDE: 180 mg/1
- PSEUDOEPHEDRINE HYDROCHLORIDE: 240 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43598-892"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43598-892
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d4e66d84-5ce8-36a1-7a99-2a2a0f38ce19