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 20 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-548
Product ID 72189-548_16752f60-655b-f727-e063-6394a90a96b6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204798
Listing Expiration 2026-12-31
Marketing Start 2024-04-19

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 72189548
Hyphenated Format 72189-548

Supplemental Identifiers

RxCUI
349401
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 ANDA204798 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 90 TABLET, FILM COATED in 1 BOTTLE (72189-548-90)
source: ndc

Packages (1)

72189-548-90 90 TABLET, FILM COATED in 1 BOTTLE (72189-548-90)

Ingredients (1)

olmesartan medoxomil (20 mg/1)

Linked Drug Pages (1)

Olmesartan Medoxomil ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "16752f60-655b-f727-e063-6394a90a96b6", "openfda": {"unii": ["6M97XTV3HD"], "rxcui": ["349401"], "spl_set_id": ["16752f60-655a-f727-e063-6394a90a96b6"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (72189-548-90)", "package_ndc": "72189-548-90", "marketing_start_date": "20240419"}], "brand_name": "Olmesartan Medoxomil", "product_id": "72189-548_16752f60-655b-f727-e063-6394a90a96b6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "72189-548", "generic_name": "Olmesartan Medoxomil", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olmesartan Medoxomil", "active_ingredients": [{"name": "OLMESARTAN MEDOXOMIL", "strength": "20 mg/1"}], "application_number": "ANDA204798", "marketing_category": "ANDA", "marketing_start_date": "20240419", "listing_expiration_date": "20261231"}