Package 71335-2283-1

Brand: levocetirizine dihydrochloride

Generic: levocetirizine dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-2283-1
Digits Only 7133522831
Product NDC 71335-2283
Description

10 TABLET in 1 BOTTLE (71335-2283-1)

Marketing

Marketing Status
Marketed Since 2023-11-30
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": "5b01fa05-d288-47ea-a02f-f27222ce09ff", "openfda": {"unii": ["SOD6A38AGA"], "rxcui": ["855172"], "spl_set_id": ["be58ca52-ab5d-4656-bfe0-bd5766235968"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE (71335-2283-1)", "package_ndc": "71335-2283-1", "marketing_start_date": "20231130"}, {"sample": false, "description": "35 TABLET in 1 BOTTLE (71335-2283-2)", "package_ndc": "71335-2283-2", "marketing_start_date": "20231130"}, {"sample": false, "description": "5 TABLET in 1 BOTTLE (71335-2283-3)", "package_ndc": "71335-2283-3", "marketing_start_date": "20231130"}], "brand_name": "levocetirizine dihydrochloride", "product_id": "71335-2283_5b01fa05-d288-47ea-a02f-f27222ce09ff", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "71335-2283", "generic_name": "levocetirizine dihydrochloride", "labeler_name": "Bryant Ranch Prepack", "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"}