Package 82804-232-30

Brand: levocetirizine dihydrochloride

Generic: levocetirizine dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 82804-232-30
Digits Only 8280423230
Product NDC 82804-232
Product ID 82804-232_9f83891c-2466-4972-b0f4-b92cc7337be3
Description

30 TABLET, FILM COATED in 1 BOTTLE (82804-232-30)

Marketing

Marketing Status
Marketed Since 2025-07-30
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": "9f83891c-2466-4972-b0f4-b92cc7337be3", "openfda": {"upc": ["0382804232307"], "unii": ["SOD6A38AGA"], "rxcui": ["855172"], "spl_set_id": ["9f83891c-2466-4972-b0f4-b92cc7337be3"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (82804-232-30)", "package_ndc": "82804-232-30", "marketing_start_date": "20250730"}], "brand_name": "Levocetirizine Dihydrochloride", "product_id": "82804-232_9f83891c-2466-4972-b0f4-b92cc7337be3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "82804-232", "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": "ANDA090199", "marketing_category": "ANDA", "marketing_start_date": "20110906", "listing_expiration_date": "20261231"}