Package 69452-465-81

Brand: cetirizine hydrochloride

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 69452-465-81
Digits Only 6945246581
Product NDC 69452-465
Product ID 69452-465_45745bf3-a132-b51a-e063-6394a90a712e
Description

400 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69452-465-81)

Marketing

Marketing Status
Marketed Since 2024-10-20
Brand cetirizine hydrochloride
Generic cetirizine hydrochloride
Sample Package No

Linked Drug Pages (1)

CETIRIZINE HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "45745bf3-a132-b51a-e063-6394a90a712e", "openfda": {"upc": ["0369458265233"], "unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["831d4141-b3be-4d98-a372-9c4d57ad296c"], "manufacturer_name": ["Bionpharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "400 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69452-465-81)", "package_ndc": "69452-465-81", "marketing_start_date": "20241020"}], "brand_name": "CETIRIZINE HYDROCHLORIDE", "product_id": "69452-465_45745bf3-a132-b51a-e063-6394a90a712e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "69452-465", "generic_name": "CETIRIZINE HYDROCHLORIDE", "labeler_name": "Bionpharma Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "CETIRIZINE HYDROCHLORIDE", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078862", "marketing_category": "ANDA", "marketing_start_date": "20241020", "listing_expiration_date": "20261231"}