losartan potassium

Generic: losartan potassium

Labeler: aphena pharma solutions - tennessee, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name losartan potassium
Generic Name losartan potassium
Labeler aphena pharma solutions - tennessee, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

losartan potassium 25 mg/1

Manufacturer
Aphena Pharma Solutions - Tennessee, LLC

Identifiers & Regulatory

Product NDC 71610-224
Product ID 71610-224_4e03cfb8-7719-4226-b4a4-10fff49b8390
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091497
Listing Expiration 2026-12-31
Marketing Start 2011-06-01

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 71610224
Hyphenated Format 71610-224

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 ANDA091497 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (71610-224-30)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71610-224-60)
  • 180 TABLET, FILM COATED in 1 BOTTLE (71610-224-80)
source: ndc

Packages (3)

71610-224-30 30 TABLET, FILM COATED in 1 BOTTLE (71610-224-30) 71610-224-60 90 TABLET, FILM COATED in 1 BOTTLE (71610-224-60) 71610-224-80 180 TABLET, FILM COATED in 1 BOTTLE (71610-224-80)

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": "4e03cfb8-7719-4226-b4a4-10fff49b8390", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979485"], "spl_set_id": ["35e3472a-457f-4f95-a78d-dbff2595171d"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71610-224-30)", "package_ndc": "71610-224-30", "marketing_start_date": "20190121"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71610-224-60)", "package_ndc": "71610-224-60", "marketing_start_date": "20190121"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (71610-224-80)", "package_ndc": "71610-224-80", "marketing_start_date": "20190121"}], "brand_name": "Losartan Potassium", "product_id": "71610-224_4e03cfb8-7719-4226-b4a4-10fff49b8390", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "71610-224", "generic_name": "Losartan Potassium", "labeler_name": "Aphena Pharma Solutions - Tennessee, 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": "20110601", "listing_expiration_date": "20261231"}