olmesartan medoxomil

Generic: olmesartan medoxomil

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

Drug Facts

Product Profile

Brand Name olmesartan medoxomil
Generic Name olmesartan medoxomil
Labeler modavar pharmaceuticals llc
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

olmesartan medoxomil 5 mg/1

Manufacturer
Modavar Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 72241-078
Product ID 72241-078_1f430fc9-bd4c-4328-a4a2-501ec991029b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210682
Listing Expiration 2026-12-31
Marketing Start 2025-07-01

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 72241078
Hyphenated Format 72241-078

Supplemental Identifiers

RxCUI
349373 349401 349405
UNII
6M97XTV3HD

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 olmesartan medoxomil (source: ndc)
Generic Name olmesartan medoxomil (source: ndc)
Application Number ANDA210682 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 90 TABLET, COATED in 1 BOTTLE (72241-078-04)
  • 500 TABLET, COATED in 1 BOTTLE (72241-078-10)
  • 1000 TABLET, COATED in 1 BOTTLE (72241-078-11)
  • 30 TABLET, COATED in 1 BOTTLE (72241-078-22)
source: ndc

Packages (4)

Ingredients (1)

olmesartan medoxomil (5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1f430fc9-bd4c-4328-a4a2-501ec991029b", "openfda": {"unii": ["6M97XTV3HD"], "rxcui": ["349373", "349401", "349405"], "spl_set_id": ["1f430fc9-bd4c-4328-a4a2-501ec991029b"], "manufacturer_name": ["Modavar Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (72241-078-04)", "package_ndc": "72241-078-04", "marketing_start_date": "20250701"}, {"sample": false, "description": "500 TABLET, COATED in 1 BOTTLE (72241-078-10)", "package_ndc": "72241-078-10", "marketing_start_date": "20250701"}, {"sample": false, "description": "1000 TABLET, COATED in 1 BOTTLE (72241-078-11)", "package_ndc": "72241-078-11", "marketing_start_date": "20250701"}, {"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (72241-078-22)", "package_ndc": "72241-078-22", "marketing_start_date": "20250701"}], "brand_name": "Olmesartan Medoxomil", "product_id": "72241-078_1f430fc9-bd4c-4328-a4a2-501ec991029b", "dosage_form": "TABLET, COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "72241-078", "generic_name": "Olmesartan Medoxomil", "labeler_name": "Modavar Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olmesartan Medoxomil", "active_ingredients": [{"name": "OLMESARTAN MEDOXOMIL", "strength": "5 mg/1"}], "application_number": "ANDA210682", "marketing_category": "ANDA", "marketing_start_date": "20250701", "listing_expiration_date": "20261231"}