olmesartan medoxomil

Generic: olmesartan medoxomil

Labeler: micro labs limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

olmesartan medoxomil 40 mg/1

Manufacturer
Micro Labs Limited

Identifiers & Regulatory

Product NDC 42571-203
Product ID 42571-203_3619c2a8-fac7-3b89-e063-6294a90a7209
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206372
Listing Expiration 2026-12-31
Marketing Start 2020-02-03

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 42571203
Hyphenated Format 42571-203

Supplemental Identifiers

RxCUI
349373 349401 349405
UPC
0342571201302 0342571203306 0342571202309
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 ANDA206372 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 500 TABLET, FILM COATED in 1 BOTTLE (42571-203-05)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (42571-203-10)
  • 10 BLISTER PACK in 1 CARTON (42571-203-11) / 10 TABLET, FILM COATED in 1 BLISTER PACK (42571-203-32)
  • 30 TABLET, FILM COATED in 1 BOTTLE (42571-203-30)
  • 90 TABLET, FILM COATED in 1 BOTTLE (42571-203-90)
source: ndc

Packages (5)

42571-203-05 500 TABLET, FILM COATED in 1 BOTTLE (42571-203-05) 42571-203-10 1000 TABLET, FILM COATED in 1 BOTTLE (42571-203-10) 42571-203-11 10 BLISTER PACK in 1 CARTON (42571-203-11) / 10 TABLET, FILM COATED in 1 BLISTER PACK (42571-203-32) 42571-203-30 30 TABLET, FILM COATED in 1 BOTTLE (42571-203-30) 42571-203-90 90 TABLET, FILM COATED in 1 BOTTLE (42571-203-90)

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": "3619c2a8-fac7-3b89-e063-6294a90a7209", "openfda": {"upc": ["0342571201302", "0342571203306", "0342571202309"], "unii": ["6M97XTV3HD"], "rxcui": ["349373", "349401", "349405"], "spl_set_id": ["de799a31-50ae-4b9e-a159-3d399b523dca"], "manufacturer_name": ["Micro Labs Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (42571-203-05)", "package_ndc": "42571-203-05", "marketing_start_date": "20200203"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (42571-203-10)", "package_ndc": "42571-203-10", "marketing_start_date": "20200203"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (42571-203-11)  / 10 TABLET, FILM COATED in 1 BLISTER PACK (42571-203-32)", "package_ndc": "42571-203-11", "marketing_start_date": "20200203"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (42571-203-30)", "package_ndc": "42571-203-30", "marketing_start_date": "20200203"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (42571-203-90)", "package_ndc": "42571-203-90", "marketing_start_date": "20200203"}], "brand_name": "OLMESARTAN MEDOXOMIL", "product_id": "42571-203_3619c2a8-fac7-3b89-e063-6294a90a7209", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "42571-203", "generic_name": "olmesartan medoxomil", "labeler_name": "Micro Labs Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OLMESARTAN MEDOXOMIL", "active_ingredients": [{"name": "OLMESARTAN MEDOXOMIL", "strength": "40 mg/1"}], "application_number": "ANDA206372", "marketing_category": "ANDA", "marketing_start_date": "20200203", "listing_expiration_date": "20261231"}