Package 85293-001-01

Brand: cetirizine hydrochloride

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 85293-001-01
Digits Only 8529300101
Product NDC 85293-001
Product ID 85293-001_2fb2f0c8-a45a-5c2a-e063-6394a90a1587
Description

100 TABLET in 1 BOTTLE (85293-001-01)

Marketing

Marketing Status
Marketed Since 2025-03-04
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": "2fb2f0c8-a45a-5c2a-e063-6394a90a1587", "openfda": {"upc": ["0385293001010"], "unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["9af4ab23-d6d3-43f9-a026-76fd9771963f"], "manufacturer_name": ["Umasuto, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (85293-001-01)", "package_ndc": "85293-001-01", "marketing_start_date": "20250304"}], "brand_name": "Cetirizine Hydrochloride", "product_id": "85293-001_2fb2f0c8-a45a-5c2a-e063-6394a90a1587", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "85293-001", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "Umasuto, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cetirizine Hydrochloride", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA077829", "marketing_category": "ANDA", "marketing_start_date": "20250304", "listing_expiration_date": "20261231"}