Package 72162-1424-2

Brand: levocetirizine dihydrochloride

Generic: levocetirizine dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1424-2
Digits Only 7216214242
Product NDC 72162-1424
Product ID 72162-1424_38cb0ddb-5227-4066-9b07-a1feececf7a3
Description

148 mL in 1 BOTTLE (72162-1424-2)

Marketing

Marketing Status
Marketed Since 2023-09-26
Brand levocetirizine dihydrochloride
Generic levocetirizine dihydrochloride
Sample Package No

Linked Drug Pages (1)

levocetirizine dihydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "38cb0ddb-5227-4066-9b07-a1feececf7a3", "openfda": {"unii": ["SOD6A38AGA"], "rxcui": ["855168"], "spl_set_id": ["a9e7152c-0aa3-4355-8805-307e510ac86b"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "148 mL in 1 BOTTLE (72162-1424-2)", "package_ndc": "72162-1424-2", "marketing_start_date": "20230926"}], "brand_name": "levocetirizine dihydrochloride", "product_id": "72162-1424_38cb0ddb-5227-4066-9b07-a1feececf7a3", "dosage_form": "SOLUTION", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "72162-1424", "generic_name": "Levocetirizine dihydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "levocetirizine dihydrochloride", "active_ingredients": [{"name": "LEVOCETIRIZINE DIHYDROCHLORIDE", "strength": ".5 mg/mL"}], "application_number": "ANDA091263", "marketing_category": "ANDA", "marketing_start_date": "20111107", "listing_expiration_date": "20261231"}