Package 63629-8500-1

Brand: levocetirizine dihydrochloride

Generic: levocetirizine dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-8500-1
Digits Only 6362985001
Product NDC 63629-8500
Product ID 63629-8500_1bfb21e7-ecfb-463f-bd30-01565cb77422
Description

30 TABLET in 1 BOTTLE (63629-8500-1)

Marketing

Marketing Status
Marketed Since 2021-05-18
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": "1bfb21e7-ecfb-463f-bd30-01565cb77422", "openfda": {"unii": ["SOD6A38AGA"], "rxcui": ["855172"], "spl_set_id": ["4d0a0f8e-b298-46d2-b27d-0bb737507fed"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (63629-8500-1)", "package_ndc": "63629-8500-1", "marketing_start_date": "20210518"}], "brand_name": "levocetirizine dihydrochloride", "product_id": "63629-8500_1bfb21e7-ecfb-463f-bd30-01565cb77422", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "63629-8500", "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/1"}], "application_number": "ANDA203646", "marketing_category": "ANDA", "marketing_start_date": "20140909", "listing_expiration_date": "20261231"}