Package 55154-2089-0

Brand: losartan potassium

Generic: losartan potassium
NDC Package

Package Facts

Identity

Package NDC 55154-2089-0
Digits Only 5515420890
Product NDC 55154-2089
Description

10 BLISTER PACK in 1 BAG (55154-2089-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2010-10-12
Brand losartan potassium
Generic losartan potassium
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "016461a7-40a7-4ebc-9342-66ea16cdb6fc", "openfda": {"upc": ["0055154478304", "0055154208901", "0055154664301"], "unii": ["3ST302B24A"], "rxcui": ["979480", "979485", "979492"], "spl_set_id": ["021cd76a-b093-4704-8410-5e7d01e20a54"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BAG (55154-2089-0)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "55154-2089-0", "marketing_start_date": "20101012"}], "brand_name": "Losartan Potassium", "product_id": "55154-2089_016461a7-40a7-4ebc-9342-66ea16cdb6fc", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "55154-2089", "generic_name": "Losartan Potassium", "labeler_name": "Cardinal Health 107, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA078243", "marketing_category": "ANDA", "marketing_start_date": "20101012", "listing_expiration_date": "20261231"}