losartan potassium

Generic: losartan potassium

Labeler: micro labs limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name losartan potassium
Generic Name losartan potassium
Labeler micro labs limited
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

losartan potassium 50 mg/1

Manufacturer
Micro Labs Limited

Identifiers & Regulatory

Product NDC 42571-111
Product ID 42571-111_38dcaa90-daef-cef7-e063-6294a90ab743
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091541
Listing Expiration 2026-12-31
Marketing Start 2012-12-06

Pharmacologic Class

Classes
angiotensin 2 receptor antagonists [moa] angiotensin 2 receptor blocker [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 42571111
Hyphenated Format 42571-111

Supplemental Identifiers

RxCUI
979480 979485 979492
UPC
0342571112301 0342571110307 0342571111304
UNII
3ST302B24A

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name losartan potassium (source: ndc)
Generic Name losartan potassium (source: ndc)
Application Number ANDA091541 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 1000 TABLET, FILM COATED in 1 BOTTLE (42571-111-10)
  • 30 TABLET, FILM COATED in 1 BOTTLE (42571-111-30)
  • 90 TABLET, FILM COATED in 1 BOTTLE (42571-111-90)
source: ndc

Packages (3)

42571-111-10 1000 TABLET, FILM COATED in 1 BOTTLE (42571-111-10) 42571-111-30 30 TABLET, FILM COATED in 1 BOTTLE (42571-111-30) 42571-111-90 90 TABLET, FILM COATED in 1 BOTTLE (42571-111-90)

Ingredients (1)

losartan potassium (50 mg/1)

Linked Drug Pages (1)

LOSARTAN POTASSIUM ndc-match (0.9)

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 (42571-111-10)", "package_ndc": "42571-111-10", "marketing_start_date": "20121206"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (42571-111-30)", "package_ndc": "42571-111-30", "marketing_start_date": "20121206"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (42571-111-90)", "package_ndc": "42571-111-90", "marketing_start_date": "20121206"}], "brand_name": "LOSARTAN POTASSIUM", "product_id": "42571-111_38dcaa90-daef-cef7-e063-6294a90ab743", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "42571-111", "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": "50 mg/1"}], "application_number": "ANDA091541", "marketing_category": "ANDA", "marketing_start_date": "20121206", "listing_expiration_date": "20261231"}