Package 82804-204-30

Brand: levocetirizine dihydrochloride

Generic: levocetirizine dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 82804-204-30
Digits Only 8280420430
Product NDC 82804-204
Product ID 82804-204_fe13f6c0-610b-43b6-8693-e9923ba405d5
Description

30 TABLET in 1 BOTTLE (82804-204-30)

Marketing

Marketing Status
Marketed Since 2025-03-07
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": "fe13f6c0-610b-43b6-8693-e9923ba405d5", "openfda": {"upc": ["0382804204304"], "unii": ["SOD6A38AGA"], "rxcui": ["855172"], "spl_set_id": ["fe13f6c0-610b-43b6-8693-e9923ba405d5"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (82804-204-30)", "package_ndc": "82804-204-30", "marketing_start_date": "20250307"}], "brand_name": "LEVOCETIRIZINE DIHYDROCHLORIDE", "product_id": "82804-204_fe13f6c0-610b-43b6-8693-e9923ba405d5", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "82804-204", "generic_name": "levocetirizine dihydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LEVOCETIRIZINE DIHYDROCHLORIDE", "active_ingredients": [{"name": "LEVOCETIRIZINE DIHYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA090385", "marketing_category": "ANDA", "marketing_start_date": "20110225", "listing_expiration_date": "20261231"}