olmesartan medoxomil
Generic: olmesartan medoxomil
Labeler: direct rxDrug Facts
Product Profile
Brand Name
olmesartan medoxomil
Generic Name
olmesartan medoxomil
Labeler
direct rx
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
olmesartan medoxomil 40 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72189-138
Product ID
72189-138_2becff06-7cc1-1200-e063-6294a90ad1ec
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA207662
Listing Expiration
2026-12-31
Marketing Start
2020-12-02
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72189138
Hyphenated Format
72189-138
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 (72189-138-30)
- 90 TABLET, FILM COATED in 1 BOTTLE (72189-138-90)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2becff06-7cc1-1200-e063-6294a90ad1ec", "openfda": {"unii": ["6M97XTV3HD"], "rxcui": ["349401", "349405"], "spl_set_id": ["b57e47a5-43e0-d1c5-e053-2a95a90a2b07"], "manufacturer_name": ["direct rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-138-30)", "package_ndc": "72189-138-30", "marketing_start_date": "20201202"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (72189-138-90)", "package_ndc": "72189-138-90", "marketing_start_date": "20201202"}], "brand_name": "OLMESARTAN MEDOXOMIL", "product_id": "72189-138_2becff06-7cc1-1200-e063-6294a90ad1ec", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "72189-138", "generic_name": "OLMESARTAN MEDOXOMIL", "labeler_name": "direct rx", "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": "20201202", "listing_expiration_date": "20261231"}