losartan potassium

Generic: losartan potassium

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

losartan potassium 100 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-097
Product ID 72189-097_2be8025a-ef51-9a86-e063-6394a90a3877
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203835
Listing Expiration 2026-12-31
Marketing Start 2022-09-27

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 72189097
Hyphenated Format 72189-097

Supplemental Identifiers

RxCUI
979480
UNII
3ST302B24A

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 ANDA203835 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (72189-097-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE (72189-097-60)
  • 90 TABLET, FILM COATED in 1 BOTTLE (72189-097-90)
source: ndc

Packages (3)

72189-097-30 30 TABLET, FILM COATED in 1 BOTTLE (72189-097-30) 72189-097-60 60 TABLET, FILM COATED in 1 BOTTLE (72189-097-60) 72189-097-90 90 TABLET, FILM COATED in 1 BOTTLE (72189-097-90)

Ingredients (1)

losartan potassium (100 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": "2be8025a-ef51-9a86-e063-6394a90a3877", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979480"], "spl_set_id": ["e9aa536e-0747-45bf-e053-2995a90ae7d6"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-097-30)", "package_ndc": "72189-097-30", "marketing_start_date": "20220927"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (72189-097-60)", "package_ndc": "72189-097-60", "marketing_start_date": "20220927"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (72189-097-90)", "package_ndc": "72189-097-90", "marketing_start_date": "20220927"}], "brand_name": "Losartan Potassium", "product_id": "72189-097_2be8025a-ef51-9a86-e063-6394a90a3877", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "72189-097", "generic_name": "Losartan Potassium", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "100 mg/1"}], "application_number": "ANDA203835", "marketing_category": "ANDA", "marketing_start_date": "20220927", "listing_expiration_date": "20261231"}