olmesartan medoxomil

Generic: olmesartan medoxomil

Labeler: lannett company, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

olmesartan medoxomil 5 mg/1

Manufacturer
Lannett Company, Inc.

Identifiers & Regulatory

Product NDC 0527-2425
Product ID 0527-2425_25a7ac1e-7dc4-3bb7-e063-6294a90ab8df
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211049
Listing Expiration 2026-12-31
Marketing Start 2019-03-05

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 05272425
Hyphenated Format 0527-2425

Supplemental Identifiers

RxCUI
349373 349401 349405
UPC
0305272425323 0305872427321
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 ANDA211049 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-2425-32)
  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-2425-46)
source: ndc

Packages (2)

0527-2425-32 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-2425-32) 0527-2425-46 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-2425-46)

Ingredients (1)

olmesartan medoxomil (5 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": "25a7ac1e-7dc4-3bb7-e063-6294a90ab8df", "openfda": {"upc": ["0305272425323", "0305872427321"], "unii": ["6M97XTV3HD"], "rxcui": ["349373", "349401", "349405"], "spl_set_id": ["c620361a-dc2d-28a1-e053-2995a90abd14"], "manufacturer_name": ["Lannett Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-2425-32)", "package_ndc": "0527-2425-32", "marketing_start_date": "20190305"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-2425-46)", "package_ndc": "0527-2425-46", "marketing_start_date": "20190305"}], "brand_name": "OLMESARTAN MEDOXOMIL", "product_id": "0527-2425_25a7ac1e-7dc4-3bb7-e063-6294a90ab8df", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "0527-2425", "generic_name": "Olmesartan medoxomil", "labeler_name": "Lannett Company, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OLMESARTAN MEDOXOMIL", "active_ingredients": [{"name": "OLMESARTAN MEDOXOMIL", "strength": "5 mg/1"}], "application_number": "ANDA211049", "marketing_category": "ANDA", "marketing_start_date": "20190305", "listing_expiration_date": "20261231"}