# Cetirizine HCl

NDC: 72657-129
Generic name: Cetirizine
Labeler / Manufacturer: GLENMARK THERAPEUTICS INC., USA
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20240513

FDA application: ANDA078427

## Active ingredients

- CETIRIZINE HYDROCHLORIDE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72657-129"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72657-129
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=04b08c52-5390-4cdb-a9e7-fca81fffdc73