# Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride

NDC: 62756-915
Generic name: Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20120929

FDA application: ANDA090922

## Active ingredients

- CETIRIZINE HYDROCHLORIDE: 5 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:"62756-915"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62756-915
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=796c4b81-145b-4050-a851-dec81ff97006