losartan potassium

Generic: losartan potassium

Labeler: xlcare pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name losartan potassium
Generic Name losartan potassium
Labeler xlcare pharmaceuticals, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

losartan potassium 100 mg/1

Manufacturer
XLCare Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72865-143
Product ID 72865-143_f26f9307-2adc-692c-e053-2995a90a83a3
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 72865143
Hyphenated Format 72865-143

Supplemental Identifiers

RxCUI
979480 979485 979492
UPC
0372865142301 0372865142905 0372865143100 0372865141106 0372865143902 0372865143308 0372865141304 0372865141908 0372865142103
UNII
3ST302B24A

Packaging Origin

Original Packager
true

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
  • 100 mg/1
source: ndc
Packaging
  • 1000 TABLET, FILM COATED in 1 BOTTLE (72865-143-10)
  • 30 TABLET, FILM COATED in 1 BOTTLE (72865-143-30)
  • 90 TABLET, FILM COATED in 1 BOTTLE (72865-143-90)
source: ndc

Packages (3)

72865-143-10 1000 TABLET, FILM COATED in 1 BOTTLE (72865-143-10) 72865-143-30 30 TABLET, FILM COATED in 1 BOTTLE (72865-143-30) 72865-143-90 90 TABLET, FILM COATED in 1 BOTTLE (72865-143-90)

Ingredients (1)

losartan potassium (100 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": "f26f9307-2adc-692c-e053-2995a90a83a3", "openfda": {"upc": ["0372865142301", "0372865142905", "0372865143100", "0372865141106", "0372865143902", "0372865143308", "0372865141304", "0372865141908", "0372865142103"], "unii": ["3ST302B24A"], "rxcui": ["979480", "979485", "979492"], "spl_set_id": ["20421665-0401-4f6e-9e1d-232c654efb0f"], "manufacturer_name": ["XLCare Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (72865-143-10)", "package_ndc": "72865-143-10", "marketing_start_date": "20200313"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72865-143-30)", "package_ndc": "72865-143-30", "marketing_start_date": "20200313"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (72865-143-90)", "package_ndc": "72865-143-90", "marketing_start_date": "20200313"}], "brand_name": "LOSARTAN POTASSIUM", "product_id": "72865-143_f26f9307-2adc-692c-e053-2995a90a83a3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "72865-143", "generic_name": "LOSARTAN POTASSIUM", "labeler_name": "XLCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LOSARTAN POTASSIUM", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "100 mg/1"}], "application_number": "ANDA203835", "marketing_category": "ANDA", "marketing_start_date": "20200313", "listing_expiration_date": "20261231"}