Package 72162-2162-2

Brand: cetirizine

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2162-2
Digits Only 7216221622
Product NDC 72162-2162
Description

300 TABLET, FILM COATED in 1 BOTTLE (72162-2162-2)

Marketing

Marketing Status
Marketed Since 2024-02-02
Brand cetirizine
Generic cetirizine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "70a5b42b-eb45-47a5-a270-afe1b83adb84", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["7e158fd6-268d-4ffc-a410-d054090d54c5"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "300 TABLET, FILM COATED in 1 BOTTLE (72162-2162-2)", "package_ndc": "72162-2162-2", "marketing_start_date": "20240202"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (72162-2162-5)", "package_ndc": "72162-2162-5", "marketing_start_date": "20240202"}], "brand_name": "Cetirizine", "product_id": "72162-2162_70a5b42b-eb45-47a5-a270-afe1b83adb84", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "72162-2162", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cetirizine", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078336", "marketing_category": "ANDA", "marketing_start_date": "20180629", "listing_expiration_date": "20261231"}