olmesartan medoxomil

Generic: olmesartan medoxomil

Labeler: sciegen pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name olmesartan medoxomil
Generic Name olmesartan medoxomil
Labeler sciegen pharmaceuticals, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

olmesartan medoxomil 5 mg/1

Manufacturer
ScieGen Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 50228-339
Product ID 50228-339_b866b8df-72d9-2de9-e053-2995a90a3d70
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208130
Listing Expiration 2026-12-31
Marketing Start 2018-06-29

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 50228339
Hyphenated Format 50228-339

Supplemental Identifiers

RxCUI
349373 349401 349405
UPC
0350228340304 0350228341301 0350228339308 0350228340908 0350228339100 0350228339902 0350228341905
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 ANDA208130 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 1000 TABLET, FILM COATED in 1 BOTTLE (50228-339-10)
  • 30 TABLET, FILM COATED in 1 BOTTLE (50228-339-30)
  • 90 TABLET, FILM COATED in 1 BOTTLE (50228-339-90)
source: ndc

Packages (3)

50228-339-10 1000 TABLET, FILM COATED in 1 BOTTLE (50228-339-10) 50228-339-30 30 TABLET, FILM COATED in 1 BOTTLE (50228-339-30) 50228-339-90 90 TABLET, FILM COATED in 1 BOTTLE (50228-339-90)

Ingredients (1)

olmesartan medoxomil (5 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": "b866b8df-72d9-2de9-e053-2995a90a3d70", "openfda": {"upc": ["0350228340304", "0350228341301", "0350228339308", "0350228340908", "0350228339100", "0350228339902", "0350228341905"], "unii": ["6M97XTV3HD"], "rxcui": ["349373", "349401", "349405"], "spl_set_id": ["f15664a4-6b5f-4e88-ad56-c827ed90a40c"], "manufacturer_name": ["ScieGen Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (50228-339-10)", "package_ndc": "50228-339-10", "marketing_start_date": "20180629"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50228-339-30)", "package_ndc": "50228-339-30", "marketing_start_date": "20180629"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50228-339-90)", "package_ndc": "50228-339-90", "marketing_start_date": "20180629"}], "brand_name": "olmesartan medoxomil", "product_id": "50228-339_b866b8df-72d9-2de9-e053-2995a90a3d70", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "50228-339", "generic_name": "olmesartan medoxomil", "labeler_name": "ScieGen Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "olmesartan medoxomil", "active_ingredients": [{"name": "OLMESARTAN MEDOXOMIL", "strength": "5 mg/1"}], "application_number": "ANDA208130", "marketing_category": "ANDA", "marketing_start_date": "20180629", "listing_expiration_date": "20261231"}