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Medicines
Spain
Fosinopril

AEMPS 2005

Fosinopril

FOSINOPRIL TEVA 20 mg COMPRIMIDOS EFG

20 mg comprimidoSpainWithdrawnAuthorised 10 May 2005

Product informationAsk Osler about it

On this page

In other countries
Packs
Documents
Sources and licences

This page is kept for reference and is not offered to search engines.

In other countries

The same active substances on other registers, the same brand first.

Apo-FosinoprilCanada · 10 MG · Tablet · Apotex INCSame form
Apo-FosinoprilCanada · 20 MG · Tablet · Apotex INCSame form
FosinoprilCanada · 20 MG · Tablet · Sanis Health INCSame form
ElitenItaly · Compressa · Bausch Health Ireland LimitedSame form
Fosinopril AurobindoItaly · Compressa · Aurobindo Pharma (Italia) S.R.L.Same form
Fosinopril Doc GenericiItaly · Compressa · Doc Generici SRLSame form

More with the same substance on this register

Fosinopril Aurovitas 20 MG Comprimidos EfgFosinopril · 20 mg · comprimidoSpain
FOSITENS 20 mg COMPRIMIDOSFosinopril · 20 mg · comprimidoSpain

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.

🇳🇱Fosinoprilnatrium Aurobindo 10 mg, tablettenNetherlands · Tablet · Aurobindo Pharma B.V.Same form

🇳🇱Fosinoprilnatrium Aurobindo 20 mg, tablettenNetherlands · Tablet · Aurobindo Pharma B.V.Same form

🇳🇱Fosinoprilnatrium Doc Generici 10 mg, tablettenNetherlands · Tablet · DOC Generici S.r.l.Same form

🇷🇸Monopril®Serbia · 20mg · tableta · Pharmaswiss D.O.O., BeogradSame form

🇷🇸Monopril®Serbia · 10mg · tableta · Pharmaswiss D.O.O., BeogradSame form

🇸🇦FOSIPRIL 10 mg tabletSaudi Arabia · Gulf Pharmaceutical Industries (Julphar)Same form

🇸🇦FOSOPRIL 10 mg tabletSaudi Arabia · Riyadh PharmaSame form

🇸🇦FOSOPRIL 20 mg tabletSaudi Arabia · Riyadh PharmaSame form

🇺🇸Fosinopril SodiumUnited States · 10MG, 20MG, 40MG · tablet · Upsher Smith LabsSame form

🇺🇸MonoprilUnited States · 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, 40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · tablet · Bristol Myers SquibbSame form

🇧🇷Fosinopril SódicoBrazil · Ranbaxy Farmacêutica LtdaSame substance

🇧🇷Fosinopril SódicoBrazil · Biolab Farma Genericos LtdaSame substance

🇧🇷FosiprazBrazil · Biolab Farma Genericos LtdaSame substance

🇷🇴FOSINOPRIL AUROBINDO 10 mgRomania · 10mg · compr. · Aurobindo Pharma Romania S.R.L.Same substance

🇷🇴FOSINOPRIL AUROBINDO 20 mgRomania · 20mg · compr. · Aurobindo Pharma Romania S.R.L.Same substance

🇷🇴MONOPRIL 10 mgRomania · 10mg · compr. · Pharmaswiss Ceská Republika S.R.O.Same substance

Packs

Pack	Code	Status
FOSINOPRIL TEVA 20 mg COMPRIMIDOS EFG , 28 comprimidos	656545

Documents

The official texts, at the regulator.

Summary of product characteristicsAEMPS
Package leafletAEMPS
Register entryAEMPS

Sources and licences

Compiled by Prognia from the public register below; the register’s text is the official one.

Agencia Española de Medicamentos y Productos Sanitarios

Fuente de la información: Agencia Española de Medicamentos y Productos Sanitarios www.aemps.gob.es; CIMA medicamentos, acquired 11 October 2026 UTC; each source response/update date retained.

Licence: AEMPS explicit public open-data reuse for citizens and companies; source attribution and update date required · Added 12 Oct 2026

Report an error or request removalCorrections from the holder or the register are welcome.

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

Active substance: Fosinopril
Strength: 20 mg
Dosage form: comprimido
Route: vía oral
Register: Spain (AEMPS)
Status: Withdrawn
Status in the register: Revocado
Authorised: 10 May 2005
Registration: 66779
Marketing authorisation holder: Teva Pharma S.L.U.
Procedure: National, MRP or DCP
Supply: Medicamento Sujeto A Prescripción Médica. Tratamiento De Larga Duración