losartan potassium

Generic: losartan potassium

Labeler: coupler llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

losartan potassium 50 mg/1

Manufacturer
Coupler LLC

Identifiers & Regulatory

Product NDC 67046-1510
Product ID 67046-1510_2d1ad3cf-2474-bcba-e063-6294a90a6054
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202230
Listing Expiration 2026-12-31
Marketing Start 2025-02-01

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 670461510
Hyphenated Format 67046-1510

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 ANDA202230 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1510-3)
source: ndc

Packages (1)

67046-1510-3 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1510-3)

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": "2d1ad3cf-2474-bcba-e063-6294a90a6054", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979492"], "spl_set_id": ["2d1b1648-8b24-cf4f-e063-6294a90afdd8"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1510-3)", "package_ndc": "67046-1510-3", "marketing_start_date": "20250201"}], "brand_name": "Losartan potassium", "product_id": "67046-1510_2d1ad3cf-2474-bcba-e063-6294a90a6054", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "67046-1510", "generic_name": "Losartan potassium", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA202230", "marketing_category": "ANDA", "marketing_start_date": "20250201", "listing_expiration_date": "20261231"}