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 50 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-4489
Product ID 50090-4489_9edec7d5-8354-46fb-837d-393ce6b7f2d8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203835
Listing Expiration 2027-12-31
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 500904489
Hyphenated Format 50090-4489

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 ANDA203835 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (50090-4489-0)
  • 90 TABLET, FILM COATED in 1 BOTTLE (50090-4489-1)
  • 100 TABLET, FILM COATED in 1 BOTTLE (50090-4489-2)
source: ndc

Packages (3)

50090-4489-0 30 TABLET, FILM COATED in 1 BOTTLE (50090-4489-0) 50090-4489-1 90 TABLET, FILM COATED in 1 BOTTLE (50090-4489-1) 50090-4489-2 100 TABLET, FILM COATED in 1 BOTTLE (50090-4489-2)

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": "9edec7d5-8354-46fb-837d-393ce6b7f2d8", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979492"], "spl_set_id": ["f29cc61a-afba-4ecb-8043-5f103872f1ae"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-4489-0)", "package_ndc": "50090-4489-0", "marketing_start_date": "20190829"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-4489-1)", "package_ndc": "50090-4489-1", "marketing_start_date": "20190829"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (50090-4489-2)", "package_ndc": "50090-4489-2", "marketing_start_date": "20230809"}], "brand_name": "Losartan Potassium", "product_id": "50090-4489_9edec7d5-8354-46fb-837d-393ce6b7f2d8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "50090-4489", "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": "50 mg/1"}], "application_number": "ANDA203835", "marketing_category": "ANDA", "marketing_start_date": "20150819", "listing_expiration_date": "20271231"}