# Cetirizine Hydrochloride

NDC: 68788-8282
Generic name: Cetirizine Hydrochloride
Labeler / Manufacturer: Preferred Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20231025

FDA application: ANDA076601

## Active ingredients

- CETIRIZINE HYDROCHLORIDE: 1 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68788-8282"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68788-8282
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7e94be37-0971-44b3-9857-f56330d810b6