olmesartan medoxomil

Generic: olmesartan medoxomil

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name olmesartan medoxomil
Generic Name olmesartan medoxomil
Labeler direct_rx
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

olmesartan medoxomil 5 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-373
Product ID 72189-373_2c4cb2f6-84b2-31c2-e063-6394a90a5568
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207662
Listing Expiration 2026-12-31
Marketing Start 2022-08-15

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 72189373
Hyphenated Format 72189-373

Supplemental Identifiers

RxCUI
349373
UNII
6M97XTV3HD

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 ANDA207662 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 90 TABLET, FILM COATED in 1 BOTTLE (72189-373-90)
source: ndc

Packages (1)

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": "2c4cb2f6-84b2-31c2-e063-6394a90a5568", "openfda": {"unii": ["6M97XTV3HD"], "rxcui": ["349373"], "spl_set_id": ["e64c3b3b-d5e7-6d46-e053-2a95a90a1b64"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (72189-373-90)", "package_ndc": "72189-373-90", "marketing_start_date": "20220815"}], "brand_name": "Olmesartan Medoxomil", "product_id": "72189-373_2c4cb2f6-84b2-31c2-e063-6394a90a5568", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "72189-373", "generic_name": "Olmesartan Medoxomil", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olmesartan Medoxomil", "active_ingredients": [{"name": "OLMESARTAN MEDOXOMIL", "strength": "5 mg/1"}], "application_number": "ANDA207662", "marketing_category": "ANDA", "marketing_start_date": "20220815", "listing_expiration_date": "20261231"}