losartan potassium tablets, 100 mg

Generic: losartan potassium

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

Drug Facts

Product Profile

Brand Name losartan potassium tablets, 100 mg
Generic Name losartan potassium
Labeler coupler llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

losartan potassium 100 mg/1

Manufacturer
Coupler LLC

Identifiers & Regulatory

Product NDC 67046-1511
Product ID 67046-1511_2d1b0335-fa55-d08f-e063-6294a90a26b3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA201170
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 670461511
Hyphenated Format 67046-1511

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 tablets, 100 mg (source: ndc)
Generic Name losartan potassium (source: ndc)
Application Number ANDA201170 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BLISTER PACK (67046-1511-3)
source: ndc

Packages (1)

Ingredients (1)

losartan potassium (100 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2d1b0335-fa55-d08f-e063-6294a90a26b3", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979480"], "spl_set_id": ["2d1b03bb-2355-baac-e063-6294a90a9b40"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (67046-1511-3)", "package_ndc": "67046-1511-3", "marketing_start_date": "20250201"}], "brand_name": "Losartan potassium Tablets, 100 mg", "product_id": "67046-1511_2d1b0335-fa55-d08f-e063-6294a90a26b3", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "67046-1511", "generic_name": "losartan potassium", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan potassium Tablets, 100 mg", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "100 mg/1"}], "application_number": "ANDA201170", "marketing_category": "ANDA", "marketing_start_date": "20250201", "listing_expiration_date": "20261231"}