Package 0615-8565-39

Brand: levocetirizine dihydrochloride

Generic: levocetirizine dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 0615-8565-39
Digits Only 0615856539
Product NDC 0615-8565
Product ID 0615-8565_edb36c02-fd49-4de3-b697-cdb6d14cd314
Description

30 TABLET in 1 BLISTER PACK (0615-8565-39)

Marketing

Marketing Status
Marketed Since 2025-02-20
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": "edb36c02-fd49-4de3-b697-cdb6d14cd314", "openfda": {"unii": ["SOD6A38AGA"], "rxcui": ["855172"], "spl_set_id": ["51d88b2a-d10d-4e7a-b874-98de48069223"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (0615-8565-39)", "package_ndc": "0615-8565-39", "marketing_start_date": "20250220"}], "brand_name": "levocetirizine dihydrochloride", "product_id": "0615-8565_edb36c02-fd49-4de3-b697-cdb6d14cd314", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "0615-8565", "generic_name": "levocetirizine dihydrochloride", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "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"}