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
Routes
ORAL
Active Ingredients

losartan potassium 50 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-2507
Product ID 72162-2507_3585dbef-6405-e0ff-e063-6394a90a3833
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203030
Listing Expiration 2026-12-31
Marketing Start 2015-10-14

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 721622507
Hyphenated Format 72162-2507

Supplemental Identifiers

RxCUI
979492
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 ANDA203030 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 1000 TABLET in 1 BOTTLE (72162-2507-0)
  • 30 TABLET in 1 BOTTLE (72162-2507-3)
  • 90 TABLET in 1 BOTTLE (72162-2507-9)
source: ndc

Packages (3)

72162-2507-0 1000 TABLET in 1 BOTTLE (72162-2507-0) 72162-2507-3 30 TABLET in 1 BOTTLE (72162-2507-3) 72162-2507-9 90 TABLET in 1 BOTTLE (72162-2507-9)

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": "3585dbef-6405-e0ff-e063-6394a90a3833", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979492"], "spl_set_id": ["3585b1d3-ccb7-747e-e063-6294a90a4b77"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (72162-2507-0)", "package_ndc": "72162-2507-0", "marketing_start_date": "20250519"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (72162-2507-3)", "package_ndc": "72162-2507-3", "marketing_start_date": "20250519"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72162-2507-9)", "package_ndc": "72162-2507-9", "marketing_start_date": "20250519"}], "brand_name": "Losartan Potassium", "product_id": "72162-2507_3585dbef-6405-e0ff-e063-6394a90a3833", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "72162-2507", "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": "50 mg/1"}], "application_number": "ANDA203030", "marketing_category": "ANDA", "marketing_start_date": "20151014", "listing_expiration_date": "20261231"}