# CETIRIZINE HYDROCHLORIDE

NDC: 55681-073
Generic name: CETIRIZINE HYDROCHLORIDE
Labeler / Manufacturer: TWIN MED, LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20220302

FDA application: ANDA209274

## 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:"55681-073"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55681-073
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=14317ee7-1061-4c2b-9427-3433e27f13f5