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
Routes
ORAL
Active Ingredients

olmesartan medoxomil 20 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-2399
Product ID 71335-2399_a638f24b-38b1-4e16-bf18-54d9b99a28d0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206720
Listing Expiration 2026-12-31
Marketing Start 2022-03-04

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 713352399
Hyphenated Format 71335-2399

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 ANDA206720 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-2399-1)
  • 60 TABLET in 1 BOTTLE (71335-2399-2)
  • 90 TABLET in 1 BOTTLE (71335-2399-3)
  • 180 TABLET in 1 BOTTLE (71335-2399-4)
source: ndc

Packages (4)

Ingredients (1)

olmesartan medoxomil (20 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a638f24b-38b1-4e16-bf18-54d9b99a28d0", "openfda": {"unii": ["6M97XTV3HD"], "rxcui": ["349401"], "spl_set_id": ["879630ff-662a-40bd-b74f-a864661dea95"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2399-1)", "package_ndc": "71335-2399-1", "marketing_start_date": "20240613"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-2399-2)", "package_ndc": "71335-2399-2", "marketing_start_date": "20240613"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-2399-3)", "package_ndc": "71335-2399-3", "marketing_start_date": "20240613"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (71335-2399-4)", "package_ndc": "71335-2399-4", "marketing_start_date": "20240613"}], "brand_name": "OLMESARTAN MEDOXOMIL", "product_id": "71335-2399_a638f24b-38b1-4e16-bf18-54d9b99a28d0", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "71335-2399", "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": "ANDA206720", "marketing_category": "ANDA", "marketing_start_date": "20220304", "listing_expiration_date": "20261231"}