# Cetirizine Hydrochloride

NDC: 0378-3635
Generic name: cetirizine hydrochloride
Labeler / Manufacturer: Mylan Pharmaceuticals Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20071227

FDA application: ANDA076677

## Active ingredients

- CETIRIZINE HYDROCHLORIDE: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0378-3635"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0378-3635
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=487ae0f0-320c-4534-b9e2-0e215f167cea