Package 71335-0940-3

Brand: levocetirizine dihydrochloride

Generic: levocetirizine dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-0940-3
Digits Only 7133509403
Product NDC 71335-0940
Description

28 TABLET in 1 BOTTLE (71335-0940-3)

Marketing

Marketing Status
Marketed Since 2018-08-30
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": "c56f1c2a-3e1a-4e1a-9b6c-855351030d80", "openfda": {"unii": ["SOD6A38AGA"], "rxcui": ["855172"], "spl_set_id": ["34541530-ae3b-4247-b08c-cd1c13e2e6a1"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-0940-1)", "package_ndc": "71335-0940-1", "marketing_start_date": "20180830"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-0940-2)", "package_ndc": "71335-0940-2", "marketing_start_date": "20180830"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (71335-0940-3)", "package_ndc": "71335-0940-3", "marketing_start_date": "20180830"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-0940-4)", "package_ndc": "71335-0940-4", "marketing_start_date": "20180830"}], "brand_name": "levocetirizine dihydrochloride", "product_id": "71335-0940_c56f1c2a-3e1a-4e1a-9b6c-855351030d80", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "71335-0940", "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": "20141027", "listing_expiration_date": "20261231"}