losartan potassium

Generic: losartan potassium

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name losartan potassium
Generic Name losartan potassium
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

losartan potassium 100 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-4712
Product ID 50090-4712_1fd5cd7c-9ae2-4c09-97fb-0c2708743423
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203835
Listing Expiration 2026-12-31
Marketing Start 2015-08-19

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 500904712
Hyphenated Format 50090-4712

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 (source: ndc)
Generic Name losartan potassium (source: ndc)
Application Number ANDA203835 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 90 TABLET, FILM COATED in 1 BOTTLE (50090-4712-0)
  • 30 TABLET, FILM COATED in 1 BOTTLE (50090-4712-1)
  • 100 TABLET, FILM COATED in 1 BOTTLE (50090-4712-2)
source: ndc

Packages (3)

50090-4712-0 90 TABLET, FILM COATED in 1 BOTTLE (50090-4712-0) 50090-4712-1 30 TABLET, FILM COATED in 1 BOTTLE (50090-4712-1) 50090-4712-2 100 TABLET, FILM COATED in 1 BOTTLE (50090-4712-2)

Ingredients (1)

losartan potassium (100 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": "1fd5cd7c-9ae2-4c09-97fb-0c2708743423", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979480"], "spl_set_id": ["27e783ce-3353-448a-b0a3-c954dfd2e4c7"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-4712-0)", "package_ndc": "50090-4712-0", "marketing_start_date": "20191112"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-4712-1)", "package_ndc": "50090-4712-1", "marketing_start_date": "20191112"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (50090-4712-2)", "package_ndc": "50090-4712-2", "marketing_start_date": "20240805"}], "brand_name": "Losartan Potassium", "product_id": "50090-4712_1fd5cd7c-9ae2-4c09-97fb-0c2708743423", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "50090-4712", "generic_name": "Losartan Potassium", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "100 mg/1"}], "application_number": "ANDA203835", "marketing_category": "ANDA", "marketing_start_date": "20150819", "listing_expiration_date": "20261231"}