olmesartan medoxomil

Generic: olmesartan medoxomil

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

olmesartan medoxomil 40 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-4053
Product ID 70518-4053_3fa20044-d4cd-ebda-e063-6294a90af1a2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208130
Listing Expiration 2026-12-31
Marketing Start 2024-04-16

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 705184053
Hyphenated Format 70518-4053

Supplemental Identifiers

RxCUI
349405
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 ANDA208130 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4053-0)
  • 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4053-1)
  • 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4053-2)
source: ndc

Packages (3)

70518-4053-0 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4053-0) 70518-4053-1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4053-1) 70518-4053-2 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4053-2)

Ingredients (1)

olmesartan medoxomil (40 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": "3fa20044-d4cd-ebda-e063-6294a90af1a2", "openfda": {"unii": ["6M97XTV3HD"], "rxcui": ["349405"], "spl_set_id": ["1be698df-30a0-4117-8c24-7253af94c8ad"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4053-0)", "package_ndc": "70518-4053-0", "marketing_start_date": "20240416"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4053-1)", "package_ndc": "70518-4053-1", "marketing_start_date": "20250320"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4053-2)", "package_ndc": "70518-4053-2", "marketing_start_date": "20250506"}], "brand_name": "olmesartan medoxomil", "product_id": "70518-4053_3fa20044-d4cd-ebda-e063-6294a90af1a2", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "70518-4053", "generic_name": "olmesartan medoxomil", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "olmesartan medoxomil", "active_ingredients": [{"name": "OLMESARTAN MEDOXOMIL", "strength": "40 mg/1"}], "application_number": "ANDA208130", "marketing_category": "ANDA", "marketing_start_date": "20240416", "listing_expiration_date": "20261231"}