Package 71335-0789-1

Brand: levocetirizine dihydrochloride

Generic: levocetirizine dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-0789-1
Digits Only 7133507891
Product NDC 71335-0789
Description

30 TABLET in 1 BOTTLE (71335-0789-1)

Marketing

Marketing Status
Marketed Since 2019-01-11
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": "4677b1a2-8516-44c2-9d61-0f033b40617c", "openfda": {"unii": ["SOD6A38AGA"], "rxcui": ["855172"], "spl_set_id": ["b7bbffcb-5f56-4735-998a-eadd07dfa2cb"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-0789-1)", "package_ndc": "71335-0789-1", "marketing_start_date": "20190111"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-0789-2)", "package_ndc": "71335-0789-2", "marketing_start_date": "20180517"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (71335-0789-3)", "package_ndc": "71335-0789-3", "marketing_start_date": "20211227"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-0789-4)", "package_ndc": "71335-0789-4", "marketing_start_date": "20211227"}], "brand_name": "Levocetirizine Dihydrochloride", "product_id": "71335-0789_4677b1a2-8516-44c2-9d61-0f033b40617c", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "71335-0789", "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": "ANDA091264", "marketing_category": "ANDA", "marketing_start_date": "20120629", "listing_expiration_date": "20261231"}