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Medicines · US (FDA)
ACE inhibitors and sartans

FDA 2013

Beta blocking agents and calcium channel blockers

Felodipine

Approved 13 Dec 2013OralTablet, extended release

The FDA lists this product in 39 strengths and forms.

Official labelAsk Osler about it

On this page

Composition
Strengths and forms
Official product information

The table holds no label text for this product yet, only the facts beside it. The official product information has the full text.

Composition

Active ingredients: FELODIPINE 10MG

Strengths and forms

The FDA lists each strength of a product separately; these pages share one label.

FELODIPINE 5MG · Tablet, extended releaseANDA203417-002 · Prescription
FELODIPINE 10MG · Tablet, extended releaseANDA203417-003 · Prescription
FELODIPINE 2.5MG · Tablet, extended releaseANDA203417-001 · Prescription
FELODIPINE 10MG · Tablet, extended releaseThis page
FELODIPINE 2.5MG · Tablet, extended releaseANDA091200-001 · Prescription
FELODIPINE 5MG · Tablet, extended releaseANDA091200-002 · Prescription
FELODIPINE 10MG · Tablet, extended releaseANDA202170-003 · Prescription
FELODIPINE 2.5MG · Tablet, extended releaseANDA202170-001 · Prescription
FELODIPINE 5MG · Tablet, extended releaseANDA202170-002 · Prescription
FELODIPINE 10MG · Tablet, extended releaseANDA090365-003 · Prescription
FELODIPINE 2.5MG · Tablet, extended releaseANDA090365-001 · Prescription

More in ACE inhibitors and sartans

Widaplikamlodipine besylate · Tablet
Sacubitril and Valsartansacubitril · Tablet

Two medicines in one question?

Name two or more medicines and Osler runs an interaction check. A severe interaction is stated at the very top of the answer.

FELODIPINE 5MG · Tablet, extended releaseANDA090365-002 · Prescription

FELODIPINE 5MG · Tablet, extended releaseANDA078855-002 · Discontinued

FELODIPINE 10MG · Tablet, extended releaseANDA078855-003 · Discontinued

FELODIPINE 2.5MG · Tablet, extended releaseANDA078855-001 · Discontinued

FELODIPINE 5MG · Tablet, extended releaseANDA204800-002 · Prescription

FELODIPINE 10MG · Tablet, extended releaseANDA204800-003 · Prescription

FELODIPINE 2.5MG · Tablet, extended releaseANDA204800-001 · Prescription

FELODIPINE 10MG · Tablet, extended releaseANDA091484-003 · Discontinued

FELODIPINE 2.5MG · Tablet, extended releaseANDA091484-001 · Discontinued

FELODIPINE 5MG · Tablet, extended releaseANDA091484-002 · Discontinued

FELODIPINE 10MG · Tablet, extended releaseANDA201964-003 · Prescription

FELODIPINE 2.5MG · Tablet, extended releaseANDA201964-001 · Prescription

FELODIPINE 5MG · Tablet, extended releaseANDA201964-002 · Prescription

FELODIPINE 5MG · Tablet, extended releaseANDA210847-002 · Prescription

FELODIPINE 10MG · Tablet, extended releaseANDA210847-003 · Prescription

FELODIPINE 2.5MG · Tablet, extended releaseANDA210847-001 · Prescription

FELODIPINE 10MG · Tablet, extended releaseANDA075896-003 · Discontinued

FELODIPINE 2.5MG · Tablet, extended releaseANDA075896-001 · Discontinued

FELODIPINE 5MG · Tablet, extended releaseANDA075896-002 · Discontinued

FELODIPINE 10MG · Tablet, extended releaseANDA203032-003 · Prescription

FELODIPINE 2.5MG · Tablet, extended releaseANDA203032-001 · Prescription

FELODIPINE 5MG · Tablet, extended releaseANDA203032-002 · Prescription

FELODIPINE 10MG · Tablet, extended releaseANDA200815-003 · Prescription

FELODIPINE 2.5MG · Tablet, extended releaseANDA200815-001 · Prescription

FELODIPINE 5MG · Tablet, extended releaseANDA200815-002 · Prescription

FELODIPINE 10MG · Tablet, extended releaseANDA203983-003 · Discontinued

FELODIPINE 2.5MG · Tablet, extended releaseANDA203983-001 · Discontinued

FELODIPINE 5MG · Tablet, extended releaseANDA203983-002 · Discontinued

Official product information

Drugs@FDA lists the approved labels, letters and reviews for application ANDA091200.

Prognia shows this product information for reference and learning. It is not treatment advice and can lag behind the official text. Always check the current product information and local protocols before prescribing.

At a glance

Brand name: Felodipine
Drug class: Beta blocking agents and calcium channel blockers, ACE inhibitors and calcium channel blockers, Dihydropyridine derivatives
Group: ACE inhibitors and sartans
Route: Oral
Dosage form: Tablet, extended release
Applicant: Sun Pharm Inds LTD
Status: Prescription
FDA approval: 13 Dec 2013
Application: ANDA091200-003
RxCUI: 4316

Guidelines

Guidelines in cardiology1,851 guidelines in the library

FDA 2024

Entresto Sprinklesacubitril · Capsule, pellets

FDA 2023Filsparisparsentan · Tablet

FDA 2021ValsartanSolution

FDA 2016Olmesartan MedoxomilTablet

FDA 2016Olmesartan Medoxomil and Hydrochlorothiazidehydrochlorothiazide · Tablet

FDA 2016Byvalsonnebivolol hydrochloride · Tablet

FDA 2015Entrestosacubitril · Tablet

FDA 2014Telmisartan and Hydrochlorothiazidehydrochlorothiazide · Tablet

FDA 2014TelmisartanTablet

FDA 2014Telmisartan and Amlodipineamlodipine besylate · Tablet

FDA 2013Epaned Kitenalapril maleate · For solution

FDA 2013Candesartan CilexetilTablet

FDA 2013Amlodipine Besylate and Valsartanamlodipine besylate · Tablet

FDA 2012Candesartan Cilexetil and Hydrochlorothiazidecandesartan cilexetil · Tablet

FDA 2012Irbesartan; Hydrochlorothiazideirbesartan: hydrochlorothiazide · Tablet

FDA 2012Amlodipine Besylate, Valsartan and Hydrochlorothiazideamlodipine besylate · Tablet