Package 42571-112-30

Brand: losartan potassium

Generic: losartan potassium
NDC Package

Package Facts

Identity

Package NDC 42571-112-30
Digits Only 4257111230
Product NDC 42571-112
Product ID 42571-112_38dcaa90-daef-cef7-e063-6294a90ab743
Description

30 TABLET, FILM COATED in 1 BOTTLE (42571-112-30)

Marketing

Marketing Status
Marketed Since 2012-12-06
Brand losartan potassium
Generic losartan potassium
Sample Package No

Linked Drug Pages (1)

LOSARTAN POTASSIUM ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "38dcaa90-daef-cef7-e063-6294a90ab743", "openfda": {"upc": ["0342571112301", "0342571110307", "0342571111304"], "unii": ["3ST302B24A"], "rxcui": ["979480", "979485", "979492"], "spl_set_id": ["f2f2b6c6-0ab1-483f-b4a2-78dfe3200153"], "manufacturer_name": ["Micro Labs Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (42571-112-10)", "package_ndc": "42571-112-10", "marketing_start_date": "20121206"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (42571-112-30)", "package_ndc": "42571-112-30", "marketing_start_date": "20121206"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (42571-112-90)", "package_ndc": "42571-112-90", "marketing_start_date": "20121206"}], "brand_name": "LOSARTAN POTASSIUM", "product_id": "42571-112_38dcaa90-daef-cef7-e063-6294a90ab743", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "42571-112", "generic_name": "losartan potassium", "labeler_name": "Micro Labs Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LOSARTAN POTASSIUM", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "100 mg/1"}], "application_number": "ANDA091541", "marketing_category": "ANDA", "marketing_start_date": "20121206", "listing_expiration_date": "20261231"}