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 25 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7794
Product ID 50090-7794_ec15d5dc-b748-428b-8f9d-bbf58c3db681
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 500907794
Hyphenated Format 50090-7794

Supplemental Identifiers

RxCUI
979485
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
  • 25 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (50090-7794-0)
  • 90 TABLET, FILM COATED in 1 BOTTLE (50090-7794-1)
  • 100 TABLET, FILM COATED in 1 BOTTLE (50090-7794-2)
source: ndc

Packages (3)

50090-7794-0 30 TABLET, FILM COATED in 1 BOTTLE (50090-7794-0) 50090-7794-1 90 TABLET, FILM COATED in 1 BOTTLE (50090-7794-1) 50090-7794-2 100 TABLET, FILM COATED in 1 BOTTLE (50090-7794-2)

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": "ec15d5dc-b748-428b-8f9d-bbf58c3db681", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979485"], "spl_set_id": ["67ffab1a-9e80-48dd-a6c6-1b586161fe50"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-7794-0)", "package_ndc": "50090-7794-0", "marketing_start_date": "20251125"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-7794-1)", "package_ndc": "50090-7794-1", "marketing_start_date": "20251125"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (50090-7794-2)", "package_ndc": "50090-7794-2", "marketing_start_date": "20251125"}], "brand_name": "Losartan Potassium", "product_id": "50090-7794_ec15d5dc-b748-428b-8f9d-bbf58c3db681", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "50090-7794", "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": "25 mg/1"}], "application_number": "ANDA203835", "marketing_category": "ANDA", "marketing_start_date": "20150819", "listing_expiration_date": "20261231"}