Regulatory PathRegulatory requirements compared

Active substance

Felodipine

Open in the medicines table

SFDA Saudi Arabia — SFDA human drug list

Trade nameStrengthForm · routePackPublic priceTypeCompanyStatus
PLENDIL 10MG S.R.TAB10 mgProlonged-release tablet · Oral use30 BlisterSAR 42.85NCE · PrescriptionAstraZenecaWithdrawn by MAH · Not Marketed
PLENDIL 5MG S.R. TAB5 mgProlonged-release tablet · Oral use30 BlisterSAR 23.80NCE · PrescriptionAstraZenecaWithdrawn by MAH · Not Marketed

US FDA United States — FDA approvals (Drugs@FDA)

ProductStrengthForm · routeApplicantStatusFirst approved
FELODIPINE2.5MG; 5MG; 10MGtablet, extended release · oralGLENMARK PHARMS LTDPrescription17 Dec 2010
FELODIPINE2.5MG; 5MG; 10MGtablet, extended release · oralPH HEALTHPrescription28 Oct 2011
FELODIPINE2.5MG; 5MG; 10MGtablet, extended release · oralTORRENT PHARMS LTDPrescription28 Nov 2011
FELODIPINE2.5MG; 5MG; 10MGtablet, extended release · oralAUROBINDO PHARMA LTDPrescription17 Jan 2013
FELODIPINE2.5MG; 5MG; 10MGtablet, extended release · oralHERITAGEPrescription8 Nov 2013
FELODIPINE2.5MG; 5MG; 10MGtablet, extended release · oralSUN PHARM INDS LTDPrescription13 Dec 2013
FELODIPINE2.5MG; 5MG; 10MGtablet, extended release · oralORBION PHARMSPrescription21 May 2015
FELODIPINE2.5MG; 5MG; 10MGtablet, extended release · oralYILINGPrescription26 Oct 2018
FELODIPINE2.5MG; 5MG; 10MGtablet, extended release · oralYUNG SHIN PHARMPrescription29 Apr 2019
PLENDIL5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**; 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**; 2.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**tablet, extended release · oralASTRAZENECADiscontinued25 Jul 1991
FELODIPINE2.5MG; 5MG; 10MGtablet, extended release · oralSUN PHARM INDUSTRIESDiscontinued2 Nov 2004
FELODIPINE2.5MG; 5MG; 10MGtablet, extended release · oralMYLANDiscontinued17 Apr 2008
FELODIPINE2.5MG; 5MG; 10MGtablet, extended release · oralWOCKHARDT BIO AGDiscontinued15 Aug 2012
FELODIPINE2.5MG; 5MG; 10MGtablet, extended release · oralJUBILANT GENERICSDiscontinued19 Aug 2016

Canada Canada — marketed products (Health Canada)

BrandDINStrengthForm · routeCompany
APO-FELODIPINE024523672.5 MGTABLET (EXTENDED-RELEASE) · ORALAPOTEX INC
APO-FELODIPINE024523755 MGTABLET (EXTENDED-RELEASE) · ORALAPOTEX INC
APO-FELODIPINE0245238310 MGTABLET (EXTENDED-RELEASE) · ORALAPOTEX INC
PLENDIL008517795 MGTABLET (EXTENDED-RELEASE) · ORALGLENWOOD GMBH PHARMAZEUTISCHE ERZEUGNISSE
PLENDIL0085178710 MGTABLET (EXTENDED-RELEASE) · ORALGLENWOOD GMBH PHARMAZEUTISCHE ERZEUGNISSE
PLENDIL020577782.5 MGTABLET (EXTENDED-RELEASE) · ORALGLENWOOD GMBH PHARMAZEUTISCHE ERZEUGNISSE
SANDOZ FELODIPINE022802645 MGTABLET (EXTENDED-RELEASE) · ORALSANDOZ CANADA INCORPORATED
SANDOZ FELODIPINE0228027210 MGTABLET (EXTENDED-RELEASE) · ORALSANDOZ CANADA INCORPORATED

Prices — United States and England

SourceProduct as listedPriceUnit / packDate
US NADACFELODIPINE ER 10 MG TABLET$0.13524per EA23 Sep 2026
US NADACFELODIPINE ER 2.5 MG TABLET$0.12686per EA23 Sep 2026
US NADACFELODIPINE ER 5 MG TABLET$0.12262per EA23 Sep 2026
NHS Drug TariffFelodipine 10mg modified-release tablets£3.6128 tablet1 Oct 2026
NHS Drug TariffFelodipine 2.5mg modified-release tablets£4.2628 tablet1 Oct 2026
NHS Drug TariffFelodipine 5mg modified-release tablets£2.9028 tablet1 Oct 2026

NADAC: average price US retail pharmacies pay to buy the medicine. NHS Drug Tariff Part VIIIA: basic price reimbursed to pharmacies in England and Wales.

Values as published by each source: SFDA human drug list (4-2026, as published by the Council of Health Insurance; indications from the CHI Daman Drug Formulary), Drugs@FDA, EMA medicines data, Health Canada Drug Product Database (Open Government Licence – Canada), CMS NADAC, NHS Drug Tariff Part VIIIA (NHSBSA Copyright, Open Government Licence v3.0), WHO Model List of Essential Medicines (CC BY 3.0 IGO; regrouped by active substance, not created by WHO), EMA PRAC, US FDA safety-related labeling changes and MHRA Drug Safety Update (Open Government Licence v3.0). Sources and reuse. Not a substitute for the official registers or the product information.