Package 50090-6979-0

Brand: levocetirizine dihydrochloride

Generic: levocetirizine dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-6979-0
Digits Only 5009069790
Product NDC 50090-6979
Product ID 50090-6979_20e6ad84-17d4-4fb3-aaa1-ee040f102f5b
Description

90 TABLET in 1 BOTTLE (50090-6979-0)

Marketing

Marketing Status
Marketed Since 2023-12-26
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": "20e6ad84-17d4-4fb3-aaa1-ee040f102f5b", "openfda": {"unii": ["SOD6A38AGA"], "rxcui": ["855172"], "spl_set_id": ["7c163007-7e0d-4d55-8ae1-89defe55580f"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-6979-0)", "package_ndc": "50090-6979-0", "marketing_start_date": "20231226"}], "brand_name": "Levocetirizine Dihydrochloride", "product_id": "50090-6979_20e6ad84-17d4-4fb3-aaa1-ee040f102f5b", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "50090-6979", "generic_name": "Levocetirizine Dihydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levocetirizine Dihydrochloride", "active_ingredients": [{"name": "LEVOCETIRIZINE DIHYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA091264", "marketing_category": "ANDA", "marketing_start_date": "20120629", "listing_expiration_date": "20261231"}