amlodipine and olmesartan medoxomil

Generic: amlodipine and olmesartan medoxomil

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

Drug Facts

Product Profile

Brand Name amlodipine and olmesartan medoxomil
Generic Name amlodipine and olmesartan medoxomil
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

amlodipine besylate 5 mg/1, olmesartan medoxomil 20 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-2379
Product ID 72162-2379_e325e45e-7520-4aee-88c4-6ad36ecb37c9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207435
Listing Expiration 2026-12-31
Marketing Start 2018-01-01

Pharmacologic Class

Classes
angiotensin 2 receptor antagonists [moa] angiotensin 2 receptor blocker [epc] calcium channel antagonists [moa] calcium channel blocker [epc] cytochrome p450 3a inhibitors [moa] dihydropyridine calcium channel blocker [epc] dihydropyridines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 721622379
Hyphenated Format 72162-2379

Supplemental Identifiers

RxCUI
730869
UNII
864V2Q084H 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 amlodipine and olmesartan medoxomil (source: ndc)
Generic Name amlodipine and olmesartan medoxomil (source: ndc)
Application Number ANDA207435 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (72162-2379-3)
  • 90 TABLET in 1 BOTTLE (72162-2379-9)
source: ndc

Packages (2)

72162-2379-3 30 TABLET in 1 BOTTLE (72162-2379-3) 72162-2379-9 90 TABLET in 1 BOTTLE (72162-2379-9)

Ingredients (2)

amlodipine besylate (5 mg/1) olmesartan medoxomil (20 mg/1)

Linked Drug Pages (1)

AMLODIPINE AND OLMESARTAN MEDOXOMIL ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e325e45e-7520-4aee-88c4-6ad36ecb37c9", "openfda": {"unii": ["864V2Q084H", "6M97XTV3HD"], "rxcui": ["730869"], "spl_set_id": ["f16c4254-fb35-408e-9419-e17d684ea5ac"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72162-2379-3)", "package_ndc": "72162-2379-3", "marketing_start_date": "20240815"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72162-2379-9)", "package_ndc": "72162-2379-9", "marketing_start_date": "20240815"}], "brand_name": "AMLODIPINE AND OLMESARTAN MEDOXOMIL", "product_id": "72162-2379_e325e45e-7520-4aee-88c4-6ad36ecb37c9", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]", "Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A Inhibitors [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "72162-2379", "generic_name": "Amlodipine and Olmesartan Medoxomil", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AMLODIPINE AND OLMESARTAN MEDOXOMIL", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "5 mg/1"}, {"name": "OLMESARTAN MEDOXOMIL", "strength": "20 mg/1"}], "application_number": "ANDA207435", "marketing_category": "ANDA", "marketing_start_date": "20180101", "listing_expiration_date": "20261231"}