olmesartan medoxomil

Generic: olmesartan medoxomil

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name olmesartan medoxomil
Generic Name olmesartan medoxomil
Labeler proficient rx lp
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

olmesartan medoxomil 20 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-172
Product ID 71205-172_bfc9129b-05ad-4ae3-b701-73f9cc0ae9e1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204798
Listing Expiration 2026-12-31
Marketing Start 2017-04-24

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 71205172
Hyphenated Format 71205-172

Supplemental Identifiers

RxCUI
349401 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 ANDA204798 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (71205-172-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71205-172-60)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71205-172-90)
source: ndc

Packages (3)

71205-172-30 30 TABLET, FILM COATED in 1 BOTTLE (71205-172-30) 71205-172-60 60 TABLET, FILM COATED in 1 BOTTLE (71205-172-60) 71205-172-90 90 TABLET, FILM COATED in 1 BOTTLE (71205-172-90)

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": "bfc9129b-05ad-4ae3-b701-73f9cc0ae9e1", "openfda": {"unii": ["6M97XTV3HD"], "rxcui": ["349401", "349405"], "spl_set_id": ["e210f962-9b91-46c6-af8f-9f9a9ae84245"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-172-30)", "package_ndc": "71205-172-30", "marketing_start_date": "20181201"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-172-60)", "package_ndc": "71205-172-60", "marketing_start_date": "20181201"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-172-90)", "package_ndc": "71205-172-90", "marketing_start_date": "20181201"}], "brand_name": "Olmesartan Medoxomil", "product_id": "71205-172_bfc9129b-05ad-4ae3-b701-73f9cc0ae9e1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "71205-172", "generic_name": "Olmesartan Medoxomil", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olmesartan Medoxomil", "active_ingredients": [{"name": "OLMESARTAN MEDOXOMIL", "strength": "20 mg/1"}], "application_number": "ANDA204798", "marketing_category": "ANDA", "marketing_start_date": "20170424", "listing_expiration_date": "20261231"}