EXFORGE Film-coated tablet Ref.[50784] Active ingredients: Amlodipine Valsartan

Source: European Medicines Agency (EU)  Revision Year: 2022  Publisher: Novartis Europharm Limited, Vista Building, Elm Park, Merrion Road, Dublin 4, Ireland

Product name and form

Exforge 5 mg/80 mg film-coated tablets.

Exforge 5 mg/160 mg film-coated tablets.

Exforge 10 mg/160 mg film-coated tablets.

Pharmaceutical Form

Film-coated tablet.

Exforge 5 mg/80 mg film-coated tablets: Dark yellow, round film-coated tablet with bevelled edges, imprinted with “NVR” on one side and “NV” on the other side.

Approximate size: diameter 8.20 mm.

Exforge 5 mg/160 mg film-coated tablets: Dark yellow, oval film-coated tablet, imprinted with “NVR” on one side and “ECE” on the other side.

Approximate size: 14.2 mm (length) x 5.7 mm (width).

Exforge 10 mg/160 mg film-coated tablets: Light yellow, oval film-coated tablet, imprinted with “NVR” on one side and “UIC” on the other side.

Approximate size: 14.2 mm (length) x 5.7 mm (width).

Qualitative and quantitative composition

Exforge 5 mg/80 mg film-coated tablets: Each film-coated tablet contains 5 mg of amlodipine (as amlodipine besylate) and 80 mg of valsartan.

Exforge 5 mg/160 mg film-coated tablets: Each film-coated tablet contains 5 mg of amlodipine (as amlodipine besylate) and 160 mg of valsartan.

Exforge 10 mg/160 mg film-coated tablets: Each film-coated tablet contains 10 mg of amlodipine (as amlodipine besylate) and 160 mg of valsartan.

For the full list of excipients, see section 6.1.

Active Ingredient Description
Amlodipine

Amlodipine is a calcium ion influx inhibitor of the dihydropyridine group (slow channel blocker or calcium ion antagonist) and inhibits the transmembrane influx of calcium ions into cardiac and vascular smooth muscle.

Valsartan

Valsartan is an orally active, potent, and specific angiotensin II (Ang II) receptor antagonist. It acts selectively on the AT1-receptor subtype, which is responsible for the known actions of angiotensin II.

List of Excipients

Exforge 5 mg/80 mg film-coated tablets

Tablet core:

Cellulose microcrystalline
Crospovidone (type A)
Silica, colloidal anhydrous
Magnesium stearate

Coating:

Hypromellose, substitution type 2910 (3 mPa.s)
Titanium dioxide (E171)
Iron oxide, yellow (E172)
Macrogol 4000
Talc

Exforge 5 mg/160 mg film-coated tablets

Tablet core:

Cellulose microcrystalline
Crospovidone (type A)
Silica, colloidal anhydrous
Magnesium stearate

Coating:

Hypromellose, substitution type 2910 (3 mPa.s)
Titanium dioxide (E171)
Iron oxide, yellow (E172)
Macrogol 4000
Talc

Exforge 10 mg/160 mg film-coated tablets

Tablet core:

Cellulose microcrystalline
Crospovidone (type A)
Silica, colloidal anhydrous
Magnesium stearate

Coating:

Hypromellose, substitution type 2910 (3 mPa.s)
Titanium dioxide (E171)
Iron oxide, yellow (E172)
Iron oxide, red (E172)
Macrogol 4000
Talc

Pack sizes and marketing

PVC/PVDC blisters. One blister contains 7, 10 or 14 film-coated tablets.

Pack sizes: 7, 14, 28, 30, 56, 90, 98 or 280 film-coated tablets and multipacks containing 280 (4x70 or 20x14) film-coated tablets.

PVC/PVDC perforated unit dose blisters. One blister contains 7, 10 or 14 film-coated tablets.

Pack sizes: 56, 98 or 280 film-coated tablets.

Not all pack sizes may be marketed.

Marketing authorization holder

Novartis Europharm Limited, Vista Building, Elm Park, Merrion Road, Dublin 4, Ireland

Marketing authorization dates and numbers

Exforge 5 mg/80 mg film-coated tablets:

EU/1/06/370/001
EU/1/06/370/002
EU/1/06/370/003
EU/1/06/370/004
EU/1/06/370/005
EU/1/06/370/006
EU/1/06/370/007
EU/1/06/370/008
EU/1/06/370/025
EU/1/06/370/026
EU/1/06/370/027
EU/1/06/370/034
EU/1/06/370/037

Exforge 5 mg/160 mg film-coated tablets:

EU/1/06/370/009
EU/1/06/370/010
EU/1/06/370/011
EU/1/06/370/012
EU/1/06/370/013
EU/1/06/370/014
EU/1/06/370/015
EU/1/06/370/016
EU/1/06/370/028
EU/1/06/370/029
EU/1/06/370/030
EU/1/06/370/035
EU/1/06/370/038

Exforge 10 mg/160 mg film-coated tablets:

EU/1/06/370/017
EU/1/06/370/018
EU/1/06/370/019
EU/1/06/370/020
EU/1/06/370/021
EU/1/06/370/022
EU/1/06/370/023
EU/1/06/370/024
EU/1/06/370/031
EU/1/06/370/032
EU/1/06/370/033
EU/1/06/370/036
EU/1/06/370/039

Date of first authorisation: 17 January 2007
Date of latest renewal: 22 November 2011

Drugs

Drug Countries
EXFORGE Austria, Australia, Cyprus, Germany, Ecuador, Estonia, Spain, Finland, France, Hong Kong, Croatia, Ireland, Israel, Japan, Lithuania, Mexico, Nigeria, Netherlands, New Zealand, Poland, Romania, Singapore, Tunisia, Turkey, United Kingdom, United States, South Africa

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