Package 51407-892-90

Brand: levocetirizine dihydrochloride

Generic: levocetirizine dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 51407-892-90
Digits Only 5140789290
Product NDC 51407-892
Description

90 TABLET in 1 BOTTLE (51407-892-90)

Marketing

Marketing Status
Marketed Since 2024-03-15
Brand levocetirizine dihydrochloride
Generic levocetirizine dihydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "45b17ed5-6ba3-cfa8-e063-6294a90adfb8", "openfda": {"unii": ["SOD6A38AGA"], "rxcui": ["855172"], "spl_set_id": ["163dcce7-4535-a596-e063-6394a90a634f"], "manufacturer_name": ["Golden State Medical Supply, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (51407-892-90)", "package_ndc": "51407-892-90", "marketing_start_date": "20240315"}], "brand_name": "levocetirizine dihydrochloride", "product_id": "51407-892_45b17ed5-6ba3-cfa8-e063-6294a90adfb8", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "51407-892", "generic_name": "levocetirizine dihydrochloride", "labeler_name": "Golden State Medical Supply, Inc.", "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"}