olmesartan medoxomil

Generic: olmesartan medoxomil

Labeler: camber pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

olmesartan medoxomil 40 mg/1

Manufacturer
Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-854
Product ID 31722-854_35cb69e0-7e6c-d4ee-e063-6294a90ae48c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205499
Listing Expiration 2026-12-31
Marketing Start 2025-05-23

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 31722854
Hyphenated Format 31722-854

Supplemental Identifiers

RxCUI
349373 349401 349405
UPC
0331722854306 0331722852302 0331722853309
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 ANDA205499 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (31722-854-30)
  • 90 TABLET, FILM COATED in 1 BOTTLE (31722-854-90)
source: ndc

Packages (2)

31722-854-30 30 TABLET, FILM COATED in 1 BOTTLE (31722-854-30) 31722-854-90 90 TABLET, FILM COATED in 1 BOTTLE (31722-854-90)

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": "35cb69e0-7e6c-d4ee-e063-6294a90ae48c", "openfda": {"upc": ["0331722854306", "0331722852302", "0331722853309"], "unii": ["6M97XTV3HD"], "rxcui": ["349373", "349401", "349405"], "spl_set_id": ["53b8d406-a4f3-46ee-9aec-d70f7d806876"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (31722-854-30)", "package_ndc": "31722-854-30", "marketing_start_date": "20250523"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (31722-854-90)", "package_ndc": "31722-854-90", "marketing_start_date": "20250523"}], "brand_name": "OLMESARTAN MEDOXOMIL", "product_id": "31722-854_35cb69e0-7e6c-d4ee-e063-6294a90ae48c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "31722-854", "generic_name": "OLMESARTAN MEDOXOMIL", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OLMESARTAN MEDOXOMIL", "active_ingredients": [{"name": "OLMESARTAN MEDOXOMIL", "strength": "40 mg/1"}], "application_number": "ANDA205499", "marketing_category": "ANDA", "marketing_start_date": "20250523", "listing_expiration_date": "20261231"}