olmesartan medoxomil

Generic: olmesartan medoxomil

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

olmesartan medoxomil 40 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 65862-743
Product ID 65862-743_6135c8a8-0232-4aa1-be56-8c29a444d96f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204798
Listing Expiration 2026-12-31
Marketing Start 2017-04-24

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 65862743
Hyphenated Format 65862-743

Supplemental Identifiers

RxCUI
349373 349401 349405
UPC
0365862742308 0365862743305 0365862741301
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 ANDA204798 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (65862-743-01)
  • 500 TABLET, FILM COATED in 1 BOTTLE (65862-743-05)
  • 30 TABLET, FILM COATED in 1 BOTTLE (65862-743-30)
  • 10 BLISTER PACK in 1 CARTON (65862-743-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-743-10)
  • 90 TABLET, FILM COATED in 1 BOTTLE (65862-743-90)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (65862-743-99)
source: ndc

Packages (6)

65862-743-01 100 TABLET, FILM COATED in 1 BOTTLE (65862-743-01) 65862-743-05 500 TABLET, FILM COATED in 1 BOTTLE (65862-743-05) 65862-743-30 30 TABLET, FILM COATED in 1 BOTTLE (65862-743-30) 65862-743-78 10 BLISTER PACK in 1 CARTON (65862-743-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-743-10) 65862-743-90 90 TABLET, FILM COATED in 1 BOTTLE (65862-743-90) 65862-743-99 1000 TABLET, FILM COATED in 1 BOTTLE (65862-743-99)

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": "6135c8a8-0232-4aa1-be56-8c29a444d96f", "openfda": {"upc": ["0365862742308", "0365862743305", "0365862741301"], "unii": ["6M97XTV3HD"], "rxcui": ["349373", "349401", "349405"], "spl_set_id": ["8c94d403-809b-43b9-834f-3ecd330d2dd9"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (65862-743-01)", "package_ndc": "65862-743-01", "marketing_start_date": "20170424"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (65862-743-05)", "package_ndc": "65862-743-05", "marketing_start_date": "20170424"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (65862-743-30)", "package_ndc": "65862-743-30", "marketing_start_date": "20170424"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (65862-743-78)  / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-743-10)", "package_ndc": "65862-743-78", "marketing_start_date": "20170424"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (65862-743-90)", "package_ndc": "65862-743-90", "marketing_start_date": "20170424"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (65862-743-99)", "package_ndc": "65862-743-99", "marketing_start_date": "20170424"}], "brand_name": "Olmesartan Medoxomil", "product_id": "65862-743_6135c8a8-0232-4aa1-be56-8c29a444d96f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "65862-743", "generic_name": "Olmesartan Medoxomil", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olmesartan Medoxomil", "active_ingredients": [{"name": "OLMESARTAN MEDOXOMIL", "strength": "40 mg/1"}], "application_number": "ANDA204798", "marketing_category": "ANDA", "marketing_start_date": "20170424", "listing_expiration_date": "20261231"}