losartan potassium

Generic: losartan potassium

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

losartan potassium 25 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-1174
Product ID 71335-1174_2ec9b39a-daae-48d5-9ea3-adcad2a1f0f7
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 713351174
Hyphenated Format 71335-1174

Supplemental Identifiers

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

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 90 TABLET, FILM COATED in 1 BOTTLE (71335-1174-1)
  • 30 TABLET, FILM COATED in 1 BOTTLE (71335-1174-2)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71335-1174-3)
  • 100 TABLET, FILM COATED in 1 BOTTLE (71335-1174-4)
  • 10 TABLET, FILM COATED in 1 BOTTLE (71335-1174-5)
  • 7 TABLET, FILM COATED in 1 BOTTLE (71335-1174-6)
source: ndc

Packages (6)

71335-1174-1 90 TABLET, FILM COATED in 1 BOTTLE (71335-1174-1) 71335-1174-2 30 TABLET, FILM COATED in 1 BOTTLE (71335-1174-2) 71335-1174-3 60 TABLET, FILM COATED in 1 BOTTLE (71335-1174-3) 71335-1174-4 100 TABLET, FILM COATED in 1 BOTTLE (71335-1174-4) 71335-1174-5 10 TABLET, FILM COATED in 1 BOTTLE (71335-1174-5) 71335-1174-6 7 TABLET, FILM COATED in 1 BOTTLE (71335-1174-6)

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": "2ec9b39a-daae-48d5-9ea3-adcad2a1f0f7", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979485"], "spl_set_id": ["45d0b1cc-d88d-4044-9692-c143cdf7a1b8"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-1174-1)", "package_ndc": "71335-1174-1", "marketing_start_date": "20190503"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-1174-2)", "package_ndc": "71335-1174-2", "marketing_start_date": "20190402"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-1174-3)", "package_ndc": "71335-1174-3", "marketing_start_date": "20240709"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71335-1174-4)", "package_ndc": "71335-1174-4", "marketing_start_date": "20240709"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (71335-1174-5)", "package_ndc": "71335-1174-5", "marketing_start_date": "20240709"}, {"sample": false, "description": "7 TABLET, FILM COATED in 1 BOTTLE (71335-1174-6)", "package_ndc": "71335-1174-6", "marketing_start_date": "20240709"}], "brand_name": "Losartan Potassium", "product_id": "71335-1174_2ec9b39a-daae-48d5-9ea3-adcad2a1f0f7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "71335-1174", "generic_name": "Losartan Potassium", "labeler_name": "Bryant Ranch Prepack", "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"}