losartan potassium

Generic: losartan potassium

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name losartan potassium
Generic Name losartan potassium
Labeler proficient rx lp
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

losartan potassium 50 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-281
Product ID 71205-281_3acdf264-82c4-4635-bd40-e80e6d8fb3f8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090083
Listing Expiration 2026-12-31
Marketing Start 2010-10-06

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 71205281
Hyphenated Format 71205-281

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 ANDA090083 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (71205-281-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71205-281-60)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71205-281-90)
source: ndc

Packages (3)

71205-281-30 30 TABLET, FILM COATED in 1 BOTTLE (71205-281-30) 71205-281-60 60 TABLET, FILM COATED in 1 BOTTLE (71205-281-60) 71205-281-90 90 TABLET, FILM COATED in 1 BOTTLE (71205-281-90)

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": "3acdf264-82c4-4635-bd40-e80e6d8fb3f8", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979492"], "spl_set_id": ["44050993-c20e-45d4-baeb-f77d91296168"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-281-30)", "package_ndc": "71205-281-30", "marketing_start_date": "20190601"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-281-60)", "package_ndc": "71205-281-60", "marketing_start_date": "20190601"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-281-90)", "package_ndc": "71205-281-90", "marketing_start_date": "20190601"}], "brand_name": "Losartan Potassium", "product_id": "71205-281_3acdf264-82c4-4635-bd40-e80e6d8fb3f8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "71205-281", "generic_name": "Losartan Potassium", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA090083", "marketing_category": "ANDA", "marketing_start_date": "20101006", "listing_expiration_date": "20261231"}