amlodipine and olmesartan medoxomil (50090-7863)

Drug Facts

Product Profile

Brand Name amlodipine and olmesartan medoxomil

Generic Name amlodipine and olmesartan medoxomil

Labeler a-s medication solutions

Dosage Form TABLET, FILM COATED

Routes

ORAL

Active Ingredients

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

Manufacturer

A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7863

Product ID 50090-7863_d7534eb1-2b9b-45ea-a35d-f1653a807a91

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA206906

Listing Expiration 2027-12-31

Marketing Start 2017-05-15

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 500907863

Hyphenated Format 50090-7863

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 ANDA206906 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

5 mg/1
20 mg/1

source: ndc

Packaging

30 TABLET, FILM COATED in 1 BOTTLE (50090-7863-0)

source: ndc

Packages (1)

50090-7863-0 30 TABLET, FILM COATED in 1 BOTTLE (50090-7863-0)

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": "d7534eb1-2b9b-45ea-a35d-f1653a807a91", "openfda": {"unii": ["864V2Q084H", "6M97XTV3HD"], "rxcui": ["730869"], "spl_set_id": ["350c7317-a92d-4bcb-973f-19d6de87ed83"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-7863-0)", "package_ndc": "50090-7863-0", "marketing_start_date": "20260122"}], "brand_name": "Amlodipine and Olmesartan Medoxomil", "product_id": "50090-7863_d7534eb1-2b9b-45ea-a35d-f1653a807a91", "dosage_form": "TABLET, FILM COATED", "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": "50090-7863", "generic_name": "Amlodipine and Olmesartan Medoxomil", "labeler_name": "A-S Medication Solutions", "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": "ANDA206906", "marketing_category": "ANDA", "marketing_start_date": "20170515", "listing_expiration_date": "20271231"}