olmesartan medoxomil
Generic: olmesartan medoxomil
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
olmesartan medoxomil
Generic Name
olmesartan medoxomil
Labeler
a-s medication solutions
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
olmesartan medoxomil 40 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-3487
Product ID
50090-3487_7dd35ea2-5d7c-4ada-bae7-24eb9f4e444a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA207662
Listing Expiration
2026-12-31
Marketing Start
2017-04-27
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500903487
Hyphenated Format
50090-3487
Supplemental Identifiers
RxCUI
UNII
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
ANDA207662 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 40 mg/1
Packaging
- 30 TABLET, FILM COATED in 1 BOTTLE (50090-3487-0)
- 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3487-1)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7dd35ea2-5d7c-4ada-bae7-24eb9f4e444a", "openfda": {"unii": ["6M97XTV3HD"], "rxcui": ["349405"], "spl_set_id": ["7afa79de-d42e-4429-874d-449d47a59fbe"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-3487-0)", "package_ndc": "50090-3487-0", "marketing_start_date": "20191018"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3487-1)", "package_ndc": "50090-3487-1", "marketing_start_date": "20180618"}], "brand_name": "olmesartan medoxomil", "product_id": "50090-3487_7dd35ea2-5d7c-4ada-bae7-24eb9f4e444a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "50090-3487", "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": "ANDA207662", "marketing_category": "ANDA", "marketing_start_date": "20170427", "listing_expiration_date": "20261231"}