olmesartan medoxomil

Generic: olmesartan medoxomil

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name olmesartan medoxomil
Generic Name olmesartan medoxomil
Labeler bryant ranch prepack
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

olmesartan medoxomil 20 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-0775
Product ID 71335-0775_a8d88d67-a666-4e95-b00a-b81c24e52a52
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207662
Listing Expiration 2026-12-31
Marketing Start 2017-04-27

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 713350775
Hyphenated Format 71335-0775

Supplemental Identifiers

RxCUI
349401
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 ANDA207662 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (71335-0775-1)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71335-0775-2)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71335-0775-3)
  • 180 TABLET, FILM COATED in 1 BOTTLE (71335-0775-4)
source: ndc

Packages (4)

71335-0775-1 30 TABLET, FILM COATED in 1 BOTTLE (71335-0775-1) 71335-0775-2 60 TABLET, FILM COATED in 1 BOTTLE (71335-0775-2) 71335-0775-3 90 TABLET, FILM COATED in 1 BOTTLE (71335-0775-3) 71335-0775-4 180 TABLET, FILM COATED in 1 BOTTLE (71335-0775-4)

Ingredients (1)

olmesartan medoxomil (20 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": "a8d88d67-a666-4e95-b00a-b81c24e52a52", "openfda": {"unii": ["6M97XTV3HD"], "rxcui": ["349401"], "spl_set_id": ["a4ceea38-8fff-4317-be04-8dc22222ec70"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-0775-1)", "package_ndc": "71335-0775-1", "marketing_start_date": "20180413"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-0775-2)", "package_ndc": "71335-0775-2", "marketing_start_date": "20180808"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-0775-3)", "package_ndc": "71335-0775-3", "marketing_start_date": "20200706"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (71335-0775-4)", "package_ndc": "71335-0775-4", "marketing_start_date": "20211227"}], "brand_name": "olmesartan medoxomil", "product_id": "71335-0775_a8d88d67-a666-4e95-b00a-b81c24e52a52", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "71335-0775", "generic_name": "olmesartan medoxomil", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "olmesartan medoxomil", "active_ingredients": [{"name": "OLMESARTAN MEDOXOMIL", "strength": "20 mg/1"}], "application_number": "ANDA207662", "marketing_category": "ANDA", "marketing_start_date": "20170427", "listing_expiration_date": "20261231"}