olmesartan medoxomil

Generic: olmesartan medoxomil

Labeler: macleods pharmaceuticals limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name olmesartan medoxomil
Generic Name olmesartan medoxomil
Labeler macleods pharmaceuticals limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

olmesartan medoxomil 20 mg/1

Manufacturer
Macleods Pharmaceuticals Limited

Identifiers & Regulatory

Product NDC 33342-179
Product ID 33342-179_c9d7d145-3702-4b5c-9808-c9a52636858d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204814
Listing Expiration 2026-12-31
Marketing Start 2017-04-25

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 33342179
Hyphenated Format 33342-179

Supplemental Identifiers

RxCUI
349373 349401 349405
UPC
0333342179074 0333342178077 0333342180070 0333342180100
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 ANDA204814 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (33342-179-07)
  • 90 TABLET in 1 BOTTLE (33342-179-10)
  • 10 BLISTER PACK in 1 CARTON (33342-179-12) / 10 TABLET in 1 BLISTER PACK
  • 1000 TABLET in 1 BOTTLE (33342-179-44)
source: ndc

Packages (4)

Ingredients (1)

olmesartan medoxomil (20 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c9d7d145-3702-4b5c-9808-c9a52636858d", "openfda": {"upc": ["0333342179074", "0333342178077", "0333342180070", "0333342180100"], "unii": ["6M97XTV3HD"], "rxcui": ["349373", "349401", "349405"], "spl_set_id": ["24e308cc-7cec-4054-9627-66f743ed71b0"], "manufacturer_name": ["Macleods Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (33342-179-07)", "package_ndc": "33342-179-07", "marketing_start_date": "20170425"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (33342-179-10)", "package_ndc": "33342-179-10", "marketing_start_date": "20170425"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (33342-179-12)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "33342-179-12", "marketing_start_date": "20170425"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (33342-179-44)", "package_ndc": "33342-179-44", "marketing_start_date": "20170425"}], "brand_name": "Olmesartan medoxomil", "product_id": "33342-179_c9d7d145-3702-4b5c-9808-c9a52636858d", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "33342-179", "generic_name": "Olmesartan medoxomil", "labeler_name": "Macleods Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olmesartan medoxomil", "active_ingredients": [{"name": "OLMESARTAN MEDOXOMIL", "strength": "20 mg/1"}], "application_number": "ANDA204814", "marketing_category": "ANDA", "marketing_start_date": "20170425", "listing_expiration_date": "20261231"}