olmesartan medoxomil
Generic: olmesartan medoxomil
Labeler: macleods pharmaceuticals limitedDrug Facts
Product Profile
Brand Name
olmesartan medoxomil
Generic Name
olmesartan medoxomil
Labeler
macleods pharmaceuticals limited
Dosage Form
TABLET
Routes
Active Ingredients
olmesartan medoxomil 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
33342-179
Product ID
33342-179_c9d7d145-3702-4b5c-9808-c9a52636858d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA204814
Listing Expiration
2026-12-31
Marketing Start
2017-04-25
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
33342179
Hyphenated Format
33342-179
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
ANDA204814 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (33342-179-07)
- 90 TABLET in 1 BOTTLE (33342-179-10)
- 10 BLISTER PACK in 1 CARTON (33342-179-12) / 10 TABLET in 1 BLISTER PACK
- 1000 TABLET in 1 BOTTLE (33342-179-44)
Packages (4)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c9d7d145-3702-4b5c-9808-c9a52636858d", "openfda": {"upc": ["0333342179074", "0333342178077", "0333342180070", "0333342180100"], "unii": ["6M97XTV3HD"], "rxcui": ["349373", "349401", "349405"], "spl_set_id": ["24e308cc-7cec-4054-9627-66f743ed71b0"], "manufacturer_name": ["Macleods Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (33342-179-07)", "package_ndc": "33342-179-07", "marketing_start_date": "20170425"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (33342-179-10)", "package_ndc": "33342-179-10", "marketing_start_date": "20170425"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (33342-179-12) / 10 TABLET in 1 BLISTER PACK", "package_ndc": "33342-179-12", "marketing_start_date": "20170425"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (33342-179-44)", "package_ndc": "33342-179-44", "marketing_start_date": "20170425"}], "brand_name": "Olmesartan medoxomil", "product_id": "33342-179_c9d7d145-3702-4b5c-9808-c9a52636858d", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "33342-179", "generic_name": "Olmesartan medoxomil", "labeler_name": "Macleods Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olmesartan medoxomil", "active_ingredients": [{"name": "OLMESARTAN MEDOXOMIL", "strength": "20 mg/1"}], "application_number": "ANDA204814", "marketing_category": "ANDA", "marketing_start_date": "20170425", "listing_expiration_date": "20261231"}