In other countries
The same active substances on other registers, the same brand first.
- PlendilArgentina · 10 MG, 5 MG · comprimido de liberación prolongada · Astrazeneca S.A.Same brand
- PlendilCanada · 5 MG · Tablet (Extended-Release) · Glenwood GMBH Pharmazeutische ErzeugnisseSame brand
- PlendilCanada · 10 MG · Tablet (Extended-Release) · Glenwood GMBH Pharmazeutische ErzeugnisseSame brand
- PlendilCanada · 2.5 MG · Tablet (Extended-Release) · Glenwood GMBH Pharmazeutische ErzeugnisseSame brand
- PLENDIL 5 mg COMPRIMIDOS DE LIBERACION PROLONGADASpain · 5 mg · comprimido de liberación prolongada · Glenwood Gmbh Pharmazeutische ErzeugnisseSame brand
- Plendil 2,5, tabletten met verlengde afgifte 2,5 mgNetherlands · Tablet met verlengde afgifte · Glenwood GmbH Pharmazeutische ErzeugnisseSame brand
- Plendil ERNew Zealand · Tab long-acting 2.5 mgSame brand
- PLENDIL 10 mgRomania · 10mg · compr. elib. prel. · Astrazeneca ABSame brand
- PLENDIL 5 mgRomania · 5mg · compr. elib. prel. · Astrazeneca ABSame brand
- Plendil®Serbia · 2.5mg · tableta sa produženim oslobađanjem · Evropa Lek Pharma D.O.O. BeogradSame brand
- Plendil®Serbia · 5mg · tableta sa produženim oslobađanjem · Evropa Lek Pharma D.O.O. BeogradSame brand
- Plendil®Serbia · 5mg · tableta sa produženim oslobađanjem · Evropa Lek Pharma D.O.O. BeogradSame brand
- Plendil 10MG S.R.TabSaudi Arabia · AstraZenecaSame brand
- Plendil 5MG S.R. TabSaudi Arabia · AstraZenecaSame brand
- PLENDIL TABLET 10 mgSingapore · 10 mg · tablet, extended release · Zuellig Pharma Pte. LTD.Same brand
- PLENDIL TABLET 2.5 mgSingapore · 2.5 mg · tablet, extended release · Zuellig Pharma Pte. LTD.Same brand
- PLENDIL TABLET 5 mgSingapore · 5 mg · tablet, extended release · Zuellig Pharma Pte. LTD.Same brand
- PlendilUnited States · 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, 2.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · tablet, extended release · AstrazenecaSame brand
- FELODIPINO SANDOZ 5 mg COMPRIMIDOS DE LIBERACIÓN PROLONGADASpain · 5 mg · comprimido de liberación prolongada · Sandoz Farmaceutica S.A.Same form
- Felodipine ratiopharm 10 mg, tabletten met gereguleerde afgifteNetherlands · Tablet met gereguleerde afgifte · ratiopharm GmbHSame form
- Felodipine ratiopharm 5 mg, tabletten met gereguleerde afgifteNetherlands · Tablet met gereguleerde afgifte · ratiopharm GmbHSame form
- Felo 10 ERNew Zealand · Tab long-acting 10 mgSame form
- Felo 5 ERNew Zealand · Tab long-acting 5 mgSame form
- FelodipineUnited States · 10MG, 2.5MG, 5MG · tablet, extended release · Aurobindo Pharma LTDSame form
- FelodilBrazil · Sandoz do Brasil Indústria Farmacêutica LtdaSame substance
- FelodipinaBrazil · Laboratório Neo Química Comércio e Indústria LtdaSame substance
- FelodipinoBrazil · Sandoz do Brasil Indústria Farmacêutica LtdaSame substance
- AURONAL 10 mgRomania · 10mg · compr. film. elib. prel. · Egis Pharmaceuticals PLCSame substance
Packs
| Pack | Code | Status |
|---|---|---|
| 10 MG COMPRESSE A RILASCIO PROLUNGATO- 14 COMPRESSE IN BLISTER PVC/PVDC/AL CON CALENDARIO | 028162030 | Autorizzata |
| 5 MG COMPRESSE A RILASCIO PROLUNGATO- 28 COMPRESSE IN BLISTER PVC/PVDC/AL CON CALENDARIO | 028162042 | Autorizzata |
| 10 MG COMPRESSE A RILASCIO PROLUNGATO- 28 COMPRESSE IN BLISTER PVC/PVDC/AL CON CALENDARIO | 028162055 | Autorizzata |
| 5 MG COMPRESSE A RILASCIO PROLUNGATO- 14 COMPRESSE IN BLISTER PVC/PVDC/AL CON CALENDARIO | 028162067 | Autorizzata |
| 5 MG COMPRESSE A RILASCIO PROLUNGATO- 20 COMPRESSE IN BLISTER PVC/PVDC/AL | 028162079 | Autorizzata |
| 5 MG COMPRESSE A RILASCIO PROLUNGATO- 30 COMPRESSE IN BLISTER PVC/PVDC/AL | 028162081 | Autorizzata |
| 5 MG COMPRESSE A RILASCIO PROLUNGATO- 50 COMPRESSE IN BLISTER PVC/PVDC/AL DIVISIBILE PER DOSE UNITARIA | 028162093 | Autorizzata |
| 5 MG COMPRESSE A RILASCIO PROLUNGATO- 90 COMPRESSE IN BLISTER PVC/PVDC/AL | 028162105 | Autorizzata |
| 5 MG COMPRESSE A RILASCIO PROLUNGATO- 98 COMPRESSE IN BLISTER PVC/PVDC/AL CON CALENDARIO | 028162117 | Autorizzata |
| 5 MG COMPRESSE A RILASCIO PROLUNGATO- 100 COMPRESSE IN BLISTER PVC/PVDC/AL | 028162129 | Autorizzata |
| 5 MG COMPRESSE A RILASCIO PROLUNGATO- 30 COMPRESSE IN FLACONE HDPE | 028162131 | Autorizzata |
| 5 MG COMPRESSE A RILASCIO PROLUNGATO- 100 COMPRESSE IN FLACONE HDPE | 028162143 | Autorizzata |
| 5 MG COMPRESSE A RILASCIO PROLUNGATO- 500 COMPRESSE IN FLACONE HDPE | 028162156 | Autorizzata |
| 10 MG COMPRESSE A RILASCIO PROLUNGATO- 20 COMPRESSE IN BLISTER PVC/PVDC/AL | 028162168 | Autorizzata |
| 10 MG COMPRESSE A RILASCIO PROLUNGATO- 30 COMPRESSE IN BLISTER PVC/PVDC/AL | 028162170 | Autorizzata |
| 10 MG COMPRESSE A RILASCIO PROLUNGATO- 50 COMPRESSE IN BLISTER PVC/PVDC/AL DIVISIBILE PER DOSE UNITARIA | 028162182 | Autorizzata |
| 10 MG COMPRESSE A RILASCIO PROLUNGATO- 90 COMPRESSE IN BLISTER PVC/PVDC/AL | 028162194 | Autorizzata |
| 10 MG COMPRESSE A RILASCIO PROLUNGATO- 98 COMPRESSE IN BLISTER PVC/PVDC/AL CON CALENDARIO | 028162206 | Autorizzata |
| 10 MG COMPRESSE A RILASCIO PROLUNGATO- 100 COMPRESSE IN BLISTER PVC/PVDC/AL | 028162218 | Autorizzata |
| 10 MG COMPRESSE A RILASCIO PROLUNGATO- 30 COMPRESSE IN FLACONE HDPE | 028162220 | Autorizzata |
| 10 MG COMPRESSE A RILASCIO PROLUNGATO- 100 COMPRESSE IN FLACONE HDPE | 028162232 | Autorizzata |
| 10 MG COMPRESSE A RILASCIO PROLUNGATO- 500 COMPRESSE IN FLACONE HDPE | 028162244 | Autorizzata |
Documents
The official texts, at the regulator.
Sources and licences
Compiled by Prognia from the public register below; the register’s text is the official one.
Agenzia Italiana del Farmaco (AIFA), Italy
Agenzia Italiana del Farmaco (AIFA); https://drive.aifa.gov.it/farmaci/confezioni_fornitura.csv; HTTP Last-Modified Mon, 12 Oct 2026 23:02:44 GMT; acquired 2026-10-13T17:21:16.224007+00:00; native fields retained, source identifier and role projections are adaptations.
Licence: CC BY 4.0; AIFA published open-data catalog · Added 13 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
- Felodipine
- Dosage form
- Compressa a rilascio prolungato
- Register
- Italy (AIFA)
- Status
- Authorised
- Status in the register
- Autorizzata
- Registration
- AIC 028162
- Marketing authorisation holder
- Glenwood GMBH Pharmazeutische Erzeugnisse
- ATC code
- C08CA02
- Procedure
- Procedura Mutuo riconoscimento o Decentrata
- Supply
- Medicinali soggetti a prescrizione medica