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 71610-439
Product ID 71610-439_ac858720-a7ec-4205-a13b-596c948cde60
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203835
Listing Expiration 2026-12-31
Marketing Start 2020-03-13

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 71610439
Hyphenated Format 71610-439

Supplemental Identifiers

RxCUI
979485 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
  • 25 mg/1
source: ndc
Packaging
  • 15 TABLET, FILM COATED in 1 BOTTLE (71610-439-15)
  • 30 TABLET, FILM COATED in 1 BOTTLE (71610-439-30)
  • 45 TABLET, FILM COATED in 1 BOTTLE (71610-439-45)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71610-439-60)
source: ndc

Packages (4)

71610-439-15 15 TABLET, FILM COATED in 1 BOTTLE (71610-439-15) 71610-439-30 30 TABLET, FILM COATED in 1 BOTTLE (71610-439-30) 71610-439-45 45 TABLET, FILM COATED in 1 BOTTLE (71610-439-45) 71610-439-60 90 TABLET, FILM COATED in 1 BOTTLE (71610-439-60)

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": "ac858720-a7ec-4205-a13b-596c948cde60", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979485", "979492"], "spl_set_id": ["8015c22c-d944-4a49-8721-70d0c1b98526"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (71610-439-15)", "package_ndc": "71610-439-15", "marketing_start_date": "20210427"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71610-439-30)", "package_ndc": "71610-439-30", "marketing_start_date": "20200624"}, {"sample": false, "description": "45 TABLET, FILM COATED in 1 BOTTLE (71610-439-45)", "package_ndc": "71610-439-45", "marketing_start_date": "20210315"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71610-439-60)", "package_ndc": "71610-439-60", "marketing_start_date": "20221017"}], "brand_name": "LOSARTAN POTASSIUM", "product_id": "71610-439_ac858720-a7ec-4205-a13b-596c948cde60", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "71610-439", "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": "ANDA203835", "marketing_category": "ANDA", "marketing_start_date": "20200313", "listing_expiration_date": "20261231"}