olmesartan medoxomil

Generic: olmesartan medoxomil

Labeler: ascend laboratories, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name olmesartan medoxomil
Generic Name olmesartan medoxomil
Labeler ascend laboratories, llc
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

olmesartan medoxomil 40 mg/1

Manufacturer
Ascend Laboratories, LLC

Identifiers & Regulatory

Product NDC 67877-447
Product ID 67877-447_a1d66aa9-d0fa-4d21-bba0-ff8078c2e5af
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206763
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 67877447
Hyphenated Format 67877-447

Supplemental Identifiers

RxCUI
349373 349401 349405
UPC
0367877445304
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 ANDA206763 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 500 TABLET, COATED in 1 BOTTLE (67877-447-05)
  • 1000 TABLET, COATED in 1 BOTTLE (67877-447-10)
  • 30 TABLET, COATED in 1 BOTTLE (67877-447-30)
  • 90 TABLET, COATED in 1 BOTTLE (67877-447-90)
source: ndc

Packages (4)

67877-447-05 500 TABLET, COATED in 1 BOTTLE (67877-447-05) 67877-447-10 1000 TABLET, COATED in 1 BOTTLE (67877-447-10) 67877-447-30 30 TABLET, COATED in 1 BOTTLE (67877-447-30) 67877-447-90 90 TABLET, COATED in 1 BOTTLE (67877-447-90)

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": "a1d66aa9-d0fa-4d21-bba0-ff8078c2e5af", "openfda": {"upc": ["0367877445304"], "unii": ["6M97XTV3HD"], "rxcui": ["349373", "349401", "349405"], "spl_set_id": ["142b735a-e1cd-46e1-a523-3ef061001bf9"], "manufacturer_name": ["Ascend Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, COATED in 1 BOTTLE (67877-447-05)", "package_ndc": "67877-447-05", "marketing_start_date": "20170424"}, {"sample": false, "description": "1000 TABLET, COATED in 1 BOTTLE (67877-447-10)", "package_ndc": "67877-447-10", "marketing_start_date": "20170424"}, {"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (67877-447-30)", "package_ndc": "67877-447-30", "marketing_start_date": "20170424"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (67877-447-90)", "package_ndc": "67877-447-90", "marketing_start_date": "20170424"}], "brand_name": "Olmesartan Medoxomil", "product_id": "67877-447_a1d66aa9-d0fa-4d21-bba0-ff8078c2e5af", "dosage_form": "TABLET, COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "67877-447", "generic_name": "Olmesartan Medoxomil", "labeler_name": "Ascend Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olmesartan Medoxomil", "active_ingredients": [{"name": "OLMESARTAN MEDOXOMIL", "strength": "40 mg/1"}], "application_number": "ANDA206763", "marketing_category": "ANDA", "marketing_start_date": "20170424", "listing_expiration_date": "20261231"}