olmesartan medoxomil

Generic: olmesartan medoxomil

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name olmesartan medoxomil
Generic Name olmesartan medoxomil
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

olmesartan medoxomil 40 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7681
Product ID 50090-7681_14dd93c4-2a8d-41d7-b844-66b048ef7315
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 500907681
Hyphenated Format 50090-7681

Supplemental Identifiers

RxCUI
349405
UNII
6M97XTV3HD

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
  • 40 mg/1
source: ndc
Packaging
  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-7681-0)
source: ndc

Packages (1)

50090-7681-0 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-7681-0)

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": "14dd93c4-2a8d-41d7-b844-66b048ef7315", "openfda": {"unii": ["6M97XTV3HD"], "rxcui": ["349405"], "spl_set_id": ["3c001b8d-f6c1-4316-b8c0-590b2fa7f2e5"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-7681-0)", "package_ndc": "50090-7681-0", "marketing_start_date": "20251009"}], "brand_name": "OLMESARTAN MEDOXOMIL", "product_id": "50090-7681_14dd93c4-2a8d-41d7-b844-66b048ef7315", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "50090-7681", "generic_name": "Olmesartan medoxomil", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OLMESARTAN MEDOXOMIL", "active_ingredients": [{"name": "OLMESARTAN MEDOXOMIL", "strength": "40 mg/1"}], "application_number": "ANDA211049", "marketing_category": "ANDA", "marketing_start_date": "20190305", "listing_expiration_date": "20261231"}