Package 85766-045-05

Brand: cetirizine hydrochloride

Generic: cetirizine hydrochloride tablets
NDC Package

Package Facts

Identity

Package NDC 85766-045-05
Digits Only 8576604505
Product NDC 85766-045
Product ID 85766-045_4a2c3f01-e8a9-c309-e063-6294a90a61e8
Description

500 TABLET, FILM COATED in 1 BOTTLE (85766-045-05)

Marketing

Marketing Status
Marketed Since 2025-08-02
Brand cetirizine hydrochloride
Generic cetirizine hydrochloride tablets
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": "4a2c3f01-e8a9-c309-e063-6294a90a61e8", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["d5297bdb-823c-4318-a797-5311d5cf0df8"], "manufacturer_name": ["Sportpharm LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (85766-045-05)", "package_ndc": "85766-045-05", "marketing_start_date": "20250802"}], "brand_name": "Cetirizine Hydrochloride", "product_id": "85766-045_4a2c3f01-e8a9-c309-e063-6294a90a61e8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "85766-045", "generic_name": "Cetirizine Hydrochloride Tablets", "labeler_name": "Sportpharm LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cetirizine Hydrochloride", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078343", "marketing_category": "ANDA", "marketing_start_date": "20181217", "listing_expiration_date": "20271231"}