losartan potassium

Generic: losartan potassium

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

losartan potassium 25 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 65862-201
Product ID 65862-201_1942e030-0f36-4f65-9f60-4898439afc61
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090083
Listing Expiration 2026-12-31
Marketing Start 2010-10-06

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 65862201
Hyphenated Format 65862-201

Supplemental Identifiers

RxCUI
979480 979485 979492
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 ANDA090083 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 500 TABLET, FILM COATED in 1 BOTTLE (65862-201-05)
  • 30 TABLET, FILM COATED in 1 BOTTLE (65862-201-30)
  • 90 TABLET, FILM COATED in 1 BOTTLE (65862-201-90)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (65862-201-99)
source: ndc

Packages (4)

65862-201-05 500 TABLET, FILM COATED in 1 BOTTLE (65862-201-05) 65862-201-30 30 TABLET, FILM COATED in 1 BOTTLE (65862-201-30) 65862-201-90 90 TABLET, FILM COATED in 1 BOTTLE (65862-201-90) 65862-201-99 1000 TABLET, FILM COATED in 1 BOTTLE (65862-201-99)

Ingredients (1)

losartan potassium (25 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": "1942e030-0f36-4f65-9f60-4898439afc61", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979480", "979485", "979492"], "spl_set_id": ["31366b4b-dfd6-4fda-babe-2cb3d2c14a2b"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (65862-201-05)", "package_ndc": "65862-201-05", "marketing_start_date": "20101006"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (65862-201-30)", "package_ndc": "65862-201-30", "marketing_start_date": "20190306"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (65862-201-90)", "package_ndc": "65862-201-90", "marketing_start_date": "20101006"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (65862-201-99)", "package_ndc": "65862-201-99", "marketing_start_date": "20101006"}], "brand_name": "Losartan Potassium", "product_id": "65862-201_1942e030-0f36-4f65-9f60-4898439afc61", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "65862-201", "generic_name": "Losartan Potassium", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "25 mg/1"}], "application_number": "ANDA090083", "marketing_category": "ANDA", "marketing_start_date": "20101006", "listing_expiration_date": "20261231"}