cozaar

Generic: losartan potassium

Labeler: organon llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

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

losartan potassium 50 mg/1

Manufacturer
Organon LLC

Identifiers & Regulatory

Product NDC 78206-122
Product ID 78206-122_998b309b-7dde-4d62-b902-010dd83108fe
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA020386
Listing Expiration 2027-12-31
Marketing Start 2021-06-01

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 78206122
Hyphenated Format 78206-122

Supplemental Identifiers

RxCUI
979480 979482 979485 979487 979492 979494
UPC
0378206122025 0378206121011 0378206123022
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 cozaar (source: ndc)
Generic Name losartan potassium (source: ndc)
Application Number NDA020386 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (78206-122-01)
  • 90 TABLET, FILM COATED in 1 BOTTLE (78206-122-02)
source: ndc

Packages (2)

78206-122-01 30 TABLET, FILM COATED in 1 BOTTLE (78206-122-01) 78206-122-02 90 TABLET, FILM COATED in 1 BOTTLE (78206-122-02)

Ingredients (1)

losartan potassium (50 mg/1)

Linked Drug Pages (1)

COZAAR ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "998b309b-7dde-4d62-b902-010dd83108fe", "openfda": {"upc": ["0378206122025", "0378206121011", "0378206123022"], "unii": ["3ST302B24A"], "rxcui": ["979480", "979482", "979485", "979487", "979492", "979494"], "spl_set_id": ["9949448f-c3b9-44ee-94ed-c1aca8c90f39"], "manufacturer_name": ["Organon LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (78206-122-01)", "package_ndc": "78206-122-01", "marketing_start_date": "20210601"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (78206-122-02)", "package_ndc": "78206-122-02", "marketing_start_date": "20210601"}], "brand_name": "COZAAR", "product_id": "78206-122_998b309b-7dde-4d62-b902-010dd83108fe", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "78206-122", "generic_name": "losartan potassium", "labeler_name": "Organon LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "COZAAR", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "50 mg/1"}], "application_number": "NDA020386", "marketing_category": "NDA", "marketing_start_date": "20210601", "listing_expiration_date": "20271231"}