losartan potassium

Generic: losartan potassium

Labeler: solco healthcare us, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

losartan potassium 25 mg/1

Manufacturer
Solco Healthcare US, LLC

Identifiers & Regulatory

Product NDC 43547-360
Product ID 43547-360_098aef71-90f1-40ee-b574-03dcbbad51a4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091497
Listing Expiration 2026-12-31
Marketing Start 2022-03-20

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 43547360
Hyphenated Format 43547-360

Supplemental Identifiers

RxCUI
979480 979485 979492
UPC
0343547360092 0343547361037 0343547362034
UNII
3ST302B24A

Packaging Origin

Original Packager
true

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 ANDA091497 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 90 TABLET, FILM COATED in 1 BOTTLE (43547-360-09)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (43547-360-11)
  • 500 TABLET, FILM COATED in 1 BOTTLE (43547-360-50)
source: ndc

Packages (3)

43547-360-09 90 TABLET, FILM COATED in 1 BOTTLE (43547-360-09) 43547-360-11 1000 TABLET, FILM COATED in 1 BOTTLE (43547-360-11) 43547-360-50 500 TABLET, FILM COATED in 1 BOTTLE (43547-360-50)

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": "098aef71-90f1-40ee-b574-03dcbbad51a4", "openfda": {"upc": ["0343547360092", "0343547361037", "0343547362034"], "unii": ["3ST302B24A"], "rxcui": ["979480", "979485", "979492"], "spl_set_id": ["fa0cf2c2-6238-4edd-94e2-b670b98a0da4"], "manufacturer_name": ["Solco Healthcare US, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (43547-360-09)", "package_ndc": "43547-360-09", "marketing_start_date": "20220320"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (43547-360-11)", "package_ndc": "43547-360-11", "marketing_start_date": "20220320"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (43547-360-50)", "package_ndc": "43547-360-50", "marketing_start_date": "20220320"}], "brand_name": "Losartan Potassium", "product_id": "43547-360_098aef71-90f1-40ee-b574-03dcbbad51a4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "43547-360", "generic_name": "Losartan Potassium", "labeler_name": "Solco Healthcare US, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "25 mg/1"}], "application_number": "ANDA091497", "marketing_category": "ANDA", "marketing_start_date": "20220320", "listing_expiration_date": "20261231"}