# Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride

NDC: 51660-037
Generic name: Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride
Labeler / Manufacturer: Ohm Laboratories Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20180301

FDA application: ANDA090818

## Active ingredients

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

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51660-037"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51660-037
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=87ab4578-84de-475d-a4b0-eec969f17253