# Rugby Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride

NDC: 0536-1279
Generic name: Cetirizine hydrochloride, Pseudoephedrine hydrochloride
Labeler / Manufacturer: Rugby Laboratories
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20200309

FDA application: ANDA210719

## Active ingredients

- CETIRIZINE HYDROCHLORIDE: 5 mg/1
- PSEUDOEPHEDRINE HYDROCHLORIDE: 120 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0536-1279"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0536-1279
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5c6ac9a2-4f0a-4297-9b83-988d54598f75