olmesartan medoxomil

Generic: olmesartan medoxomil

Labeler: accord healthcare inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name olmesartan medoxomil
Generic Name olmesartan medoxomil
Labeler accord healthcare inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

olmesartan medoxomil 40 mg/1

Manufacturer
Accord Healthcare Inc.

Identifiers & Regulatory

Product NDC 16729-322
Product ID 16729-322_424dbf67-5be3-2810-e063-6294a90a3558
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207662
Listing Expiration 2026-12-31
Marketing Start 2017-04-27

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 16729322
Hyphenated Format 16729-322

Supplemental Identifiers

RxCUI
349373 349401 349405
UPC
0316729320108 0316729322102
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 ANDA207662 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16729-322-10)
  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16729-322-15)
  • 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16729-322-17)
source: ndc

Packages (3)

16729-322-10 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16729-322-10) 16729-322-15 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16729-322-15) 16729-322-17 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16729-322-17)

Ingredients (1)

olmesartan medoxomil (40 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": "424dbf67-5be3-2810-e063-6294a90a3558", "openfda": {"upc": ["0316729320108", "0316729322102"], "unii": ["6M97XTV3HD"], "rxcui": ["349373", "349401", "349405"], "spl_set_id": ["e5dbca00-4e1b-4479-b829-021b11bc021e"], "manufacturer_name": ["Accord Healthcare Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16729-322-10)", "package_ndc": "16729-322-10", "marketing_start_date": "20170427"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16729-322-15)", "package_ndc": "16729-322-15", "marketing_start_date": "20170427"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16729-322-17)", "package_ndc": "16729-322-17", "marketing_start_date": "20170427"}], "brand_name": "olmesartan medoxomil", "product_id": "16729-322_424dbf67-5be3-2810-e063-6294a90a3558", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "16729-322", "generic_name": "olmesartan medoxomil", "labeler_name": "Accord Healthcare Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "olmesartan medoxomil", "active_ingredients": [{"name": "OLMESARTAN MEDOXOMIL", "strength": "40 mg/1"}], "application_number": "ANDA207662", "marketing_category": "ANDA", "marketing_start_date": "20170427", "listing_expiration_date": "20261231"}