olmesartan medoxomil

Generic: olmesartan medoxomil

Labeler: rising pharma holdings, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name olmesartan medoxomil
Generic Name olmesartan medoxomil
Labeler rising pharma holdings, inc.
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

olmesartan medoxomil 20 mg/1

Manufacturer
Rising Pharma Holdings, Inc.

Identifiers & Regulatory

Product NDC 64980-602
Product ID 64980-602_4e8b4338-7c4c-4af4-8658-660111a8b966
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208659
Listing Expiration 2026-12-31
Marketing Start 2024-03-30

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 64980602
Hyphenated Format 64980-602

Supplemental Identifiers

RxCUI
349373 349401 349405
UPC
0364980601092 0364980603034 0364980601030 0364980602037 0364980602099 0364980603096
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 ANDA208659 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET, COATED in 1 BOTTLE (64980-602-03)
  • 90 TABLET, COATED in 1 BOTTLE (64980-602-09)
source: ndc

Packages (2)

64980-602-03 30 TABLET, COATED in 1 BOTTLE (64980-602-03) 64980-602-09 90 TABLET, COATED in 1 BOTTLE (64980-602-09)

Ingredients (1)

olmesartan medoxomil (20 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": "4e8b4338-7c4c-4af4-8658-660111a8b966", "openfda": {"upc": ["0364980601092", "0364980603034", "0364980601030", "0364980602037", "0364980602099", "0364980603096"], "unii": ["6M97XTV3HD"], "rxcui": ["349373", "349401", "349405"], "spl_set_id": ["b02ff20e-3f0e-43f4-a7b5-6ce56295d023"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (64980-602-03)", "package_ndc": "64980-602-03", "marketing_start_date": "20240330"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (64980-602-09)", "package_ndc": "64980-602-09", "marketing_start_date": "20240330"}], "brand_name": "OLMESARTAN MEDOXOMIL", "product_id": "64980-602_4e8b4338-7c4c-4af4-8658-660111a8b966", "dosage_form": "TABLET, COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "64980-602", "generic_name": "olmesartan medoxomil", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OLMESARTAN MEDOXOMIL", "active_ingredients": [{"name": "OLMESARTAN MEDOXOMIL", "strength": "20 mg/1"}], "application_number": "ANDA208659", "marketing_category": "ANDA", "marketing_start_date": "20240330", "listing_expiration_date": "20261231"}