TAGRISSO Film-coated tablet Ref.[9022] Active ingredients: Osimertinib

Source: European Medicines Agency (EU)  Revision Year: 2020  Publisher: AstraZeneca AB, SE-151 85 Södertälje, Sweden

Product name and form

TAGRISSO 40 mg film-coated tablets.

TAGRISSO 80 mg film-coated tablets.

Pharmaceutical Form

Film-coated tablet (tablet).

TAGRISSO 40 mg tablets: Beige, 9 mm, round, biconvex tablet, debossed with “AZ” and “40” on one side and plain on the reverse.

TAGRISSO 80 mg tablets: Beige, 7.25 × 14.5 mm, oval, biconvex tablet, debossed with “AZ” and “80” on one side and plain on the reverse.

Qualitative and quantitative composition

TAGRISSO 40 mg tablets: Each tablet contains 40 mg osimertinib (as mesylate).

TAGRISSO 80 mg tablets: Each tablet contains 80 mg osimertinib (as mesylate).

Excipient with known effect: This medicine contains 0.3 mg sodium per 40 mg tablet and 0.6 mg sodium per 80 mg tablet.

For the full list of excipients, see section 6.1.

Active Ingredient Description
Osimertinib

Osimertinib is a Tyrosine Kinase Inhibitor (TKI). It is an irreversible inhibitor of Epidermal Growth Factor Receptors (EGFRs) harboring sensitising-mutations (EGFRm) and TKI-resistance mutation T790M. In vitro studies have demonstrated that osimertinib has high potency and inhibitory activity against EGFR across a range of all clinically relevant EGFR sensitising-mutant and T790M mutant non-small cell lung cancer (NSCLC) cell lines.

List of Excipients

Tablet core:

Mannitol
Microcrystalline cellulose
Low-substituted hydroxypropyl cellulose
Sodium stearyl fumarate

Tablet coating:

Polyvinyl alcohol
Titanium dioxide (E171)
Macrogol 3350
Talc
Yellow iron oxide (E172)
Red iron oxide (E172)
Black iron oxide (E172)

Pack sizes and marketing

Al/Al perforated unit dose blisters. Cartons of 30 × 1 tablets (3 blisters).

Al/Al perforated unit dose blisters. Cartons of 28 × 1 tablets (4 blisters).

Not all pack sizes may be marketed.

Marketing authorization holder

AstraZeneca AB, SE-151 85 Södertälje, Sweden

Marketing authorization dates and numbers

EU/1/16/1086/001
EU/1/16/1086/002
EU/1/16/1086/003
EU/1/16/1086/004

Date of first authorisation: 2 February 2016

Date of latest renewal: 12 December 2016

Drugs

Drug Countries
TAGRISSO Austria, Australia, Brazil, Canada, Cyprus, Ecuador, Estonia, Spain, Finland, France, Hong Kong, Croatia, Ireland, Israel, Italy, Japan, Lithuania, Netherlands, New Zealand, Poland, Romania, Singapore, Turkey, United Kingdom, United States, South Africa

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