olmesartan medoxomil (72205-166)

Drug Facts

Product Profile

Brand Name olmesartan medoxomil

Generic Name olmesartan medoxomil

Labeler novadoz pharmaceuticals llc

Dosage Form TABLET, FILM COATED

Routes

ORAL

Active Ingredients

olmesartan medoxomil 20 mg/1

Manufacturer

Novadoz Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 72205-166

Product ID 72205-166_c81a0bea-32c1-4a0a-ac3c-5afe99cecdf2

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA217399

Listing Expiration 2026-12-31

Marketing Start 2023-01-18

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 72205166

Hyphenated Format 72205-166

Supplemental Identifiers

RxCUI

349373 349401 349405

UPC

0372205166660 0372205165908 0372205166905 0372205167902 0372205165663 0372205166301 0372205167308 0372205165304 0372205167667

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 ANDA217399 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

20 mg/1

source: ndc

Packaging

30 TABLET, FILM COATED in 1 BOTTLE (72205-166-30)
1000 TABLET, FILM COATED in 1 BOTTLE (72205-166-66)
90 TABLET, FILM COATED in 1 BOTTLE (72205-166-90)
10 BLISTER PACK in 1 CARTON (72205-166-99) / 10 TABLET, FILM COATED in 1 BLISTER PACK (72205-166-11)

source: ndc

Packages (4)

72205-166-30 30 TABLET, FILM COATED in 1 BOTTLE (72205-166-30) 72205-166-66 1000 TABLET, FILM COATED in 1 BOTTLE (72205-166-66) 72205-166-90 90 TABLET, FILM COATED in 1 BOTTLE (72205-166-90) 72205-166-99 10 BLISTER PACK in 1 CARTON (72205-166-99) / 10 TABLET, FILM COATED in 1 BLISTER PACK (72205-166-11)

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": "c81a0bea-32c1-4a0a-ac3c-5afe99cecdf2", "openfda": {"upc": ["0372205166660", "0372205165908", "0372205166905", "0372205167902", "0372205165663", "0372205166301", "0372205167308", "0372205165304", "0372205167667"], "unii": ["6M97XTV3HD"], "rxcui": ["349373", "349401", "349405"], "spl_set_id": ["4238a064-1bfd-4ce3-b9d9-12c96eee8af0"], "manufacturer_name": ["Novadoz Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72205-166-30)", "package_ndc": "72205-166-30", "marketing_start_date": "20231218"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (72205-166-66)", "package_ndc": "72205-166-66", "marketing_start_date": "20240216"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (72205-166-90)", "package_ndc": "72205-166-90", "marketing_start_date": "20231218"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (72205-166-99)  / 10 TABLET, FILM COATED in 1 BLISTER PACK (72205-166-11)", "package_ndc": "72205-166-99", "marketing_start_date": "20231218"}], "brand_name": "Olmesartan medoxomil", "product_id": "72205-166_c81a0bea-32c1-4a0a-ac3c-5afe99cecdf2", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "72205-166", "generic_name": "Olmesartan medoxomil", "labeler_name": "Novadoz Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olmesartan medoxomil", "active_ingredients": [{"name": "OLMESARTAN MEDOXOMIL", "strength": "20 mg/1"}], "application_number": "ANDA217399", "marketing_category": "ANDA", "marketing_start_date": "20230118", "listing_expiration_date": "20261231"}