losartan potassium

Generic: losartan potassium

Labeler: novadoz pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name losartan potassium
Generic Name losartan potassium
Labeler novadoz pharmaceuticals llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

losartan potassium 25 mg/1

Manufacturer
Novadoz Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 72205-141
Product ID 72205-141_965852b8-5563-4f23-8cd1-a2f82cf16d3f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217396
Listing Expiration 2027-12-31
Marketing Start 2023-08-14

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 72205141
Hyphenated Format 72205-141

Supplemental Identifiers

RxCUI
979480 979485 979492
UPC
0372205142909 0372205143906 0372205142305 0372205141995 0372205141902 0372205143302 0372205142992
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 ANDA217396 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 90 TABLET, FILM COATED in 1 BOTTLE (72205-141-90)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (72205-141-99)
source: ndc

Packages (2)

72205-141-90 90 TABLET, FILM COATED in 1 BOTTLE (72205-141-90) 72205-141-99 1000 TABLET, FILM COATED in 1 BOTTLE (72205-141-99)

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": "965852b8-5563-4f23-8cd1-a2f82cf16d3f", "openfda": {"upc": ["0372205142909", "0372205143906", "0372205142305", "0372205141995", "0372205141902", "0372205143302", "0372205142992"], "unii": ["3ST302B24A"], "rxcui": ["979480", "979485", "979492"], "spl_set_id": ["5edb843a-66ed-4950-9ed0-393e6a5d7c99"], "manufacturer_name": ["Novadoz Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (72205-141-90)", "package_ndc": "72205-141-90", "marketing_start_date": "20230816"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (72205-141-99)", "package_ndc": "72205-141-99", "marketing_start_date": "20230816"}], "brand_name": "Losartan potassium", "product_id": "72205-141_965852b8-5563-4f23-8cd1-a2f82cf16d3f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "72205-141", "generic_name": "Losartan potassium", "labeler_name": "Novadoz Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "25 mg/1"}], "application_number": "ANDA217396", "marketing_category": "ANDA", "marketing_start_date": "20230814", "listing_expiration_date": "20271231"}