Package 53209-5001-1

Brand: zyrtec allergy

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 53209-5001-1
Digits Only 5320950011
Product NDC 53209-5001
Product ID 53209-5001_37e96646-1587-1156-e063-6394a90a6b22
Description

1 TABLET, FILM COATED in 1 BLISTER PACK (53209-5001-1)

Marketing

Marketing Status
Marketed Since 2025-06-19
Brand zyrtec allergy
Generic cetirizine hydrochloride
Sample Package No

Linked Drug Pages (1)

Zyrtec Allergy ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "37e96646-1587-1156-e063-6394a90a6b22", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678", "1020026"], "spl_set_id": ["3efa421d-ea70-4b1f-95d0-7c63b6c39580"], "manufacturer_name": ["Morning Star OTC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 TABLET, FILM COATED in 1 BLISTER PACK (53209-5001-1)", "package_ndc": "53209-5001-1", "marketing_start_date": "20250619"}], "brand_name": "Zyrtec Allergy", "product_id": "53209-5001_37e96646-1587-1156-e063-6394a90a6b22", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "53209-5001", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "Morning Star OTC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Zyrtec Allergy", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "NDA019835", "marketing_category": "NDA", "marketing_start_date": "20250619", "listing_expiration_date": "20261231"}