Elexacaftor

ATC R07AX32 · 5 markets · 22 records

Elexacaftor 5 markets · 22 records Forms

AU 9 records · 5 strengths

100 mgtabletTrikafta+1TRIKAFTA 100/50/75 elexacaftor 100 mg / tezacaftor 50 mg / ivacaftor 75 mg film-coated tablet and ivacaftor 150 mg film-coated tablet blister composite pack also in GB·CA·ES unknown
50 mgtabletTrikafta+1TRIKAFTA 50/25/37.5 elexacaftor 50 mg/tezacaftor 25 mg/ivacaftor 37.5 mg film-coated tablet and ivacaftor 75 mg film-coated tablet blister pack composite pack also in GB·CA·ES unknown
100 mgpowderTrikafta+1TRIKAFTA 100/50/75 GRANULES elexacaftor 100 mg/tezacaftor 50 mg/ivacaftor 75 mg granules and ivacaftor 75 mg granules sachet composite pack also in GB·CA unknown
80 mgpowderTrikafta+1TRIKAFTA 80/40/60 GRANULES elexacaftor 80 mg/tezacaftor 40 mg/ivacaftor 60 mg granules and ivacaftor 59.5 mg granules sachet composite pack also in GB·CA unknown

Records without a stated strength · 1 Trikafta

GB 4 records · 4 strengths

100 mgtabletKaftrio 75mg/50mg/100mg tablets also in AU·CA·ES
50 mgtabletKaftrio 75mg/50mg/100mg tablets also in AU·CA·ES
100 mgpowderKaftrio 60mg/40mg/80mg granules sachets also in AU·CA
80 mgpowderKaftrio 60mg/40mg/80mg granules sachets also in AU·CA

CA 4 records · 4 strengths

100 mgtabletTrikafta also in AU·GB·ES
50 mgtabletTrikafta also in AU·GB·ES
100 mgpowderTrikafta also in AU·GB
80 mgpowderTrikafta also in AU·GB

ES 4 records · 4 strengths

100 mgtabletKaftrio 75mg/50mg/100mg tablets also in AU·GB·CA
50 mgtabletKaftrio 75mg/50mg/100mg tablets also in AU·GB·CA
100 mgliquidKaftrio 75mg/50mg/100mg tablets
80 mgliquidKaftrio 75mg/50mg/100mg tablets

EU 1 records · 1 strengths

EU centralised authorisation (EMA) — Authorised at EU level — not a record of sale in any single country. The EU register carries no strength, dosage form or pack size.

Records without a stated strength · 1 Kaftrio 75mg/50mg/100mg tablets

Side-by-side table

Strength / form / release	GB	CA	AU	ES	EU
100 mg tablet	Kaftrio 75mg/50mg/100mg tablets	Trikafta	Trikafta TRIKAFTA 100/50/75 elexacaftor 100 mg / tezacaftor 50 mg / ivacaftor 75 mg film-coated tablet and ivacaftor 150 mg film-coated tablet blister composite pack	Kaftrio 75mg/50mg/100mg tablets	not recorded
50 mg tablet	Kaftrio 75mg/50mg/100mg tablets	Trikafta	Trikafta TRIKAFTA 50/25/37.5 elexacaftor 50 mg/tezacaftor 25 mg/ivacaftor 37.5 mg film-coated tablet and ivacaftor 75 mg film-coated tablet blister pack composite pack	Kaftrio 75mg/50mg/100mg tablets	not recorded
100 mg powder	Kaftrio 60mg/40mg/80mg granules sachets	Trikafta	Trikafta TRIKAFTA 100/50/75 GRANULES elexacaftor 100 mg/tezacaftor 50 mg/ivacaftor 75 mg granules and ivacaftor 75 mg granules sachet composite pack	not recorded	not recorded
80 mg powder	Kaftrio 60mg/40mg/80mg granules sachets	Trikafta	Trikafta TRIKAFTA 80/40/60 GRANULES elexacaftor 80 mg/tezacaftor 40 mg/ivacaftor 60 mg granules and ivacaftor 59.5 mg granules sachet composite pack	not recorded	not recorded
100 mg liquid	not recorded	not recorded	not recorded	Kaftrio 75mg/50mg/100mg tablets	not recorded
80 mg liquid	not recorded	not recorded	not recorded	Kaftrio 75mg/50mg/100mg tablets	not recorded
not disclosed unknown	not recorded	not recorded	Trikafta	not recorded	Kaftrio 75mg/50mg/100mg tablets

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Each country column shows the locally registered trade names — not translations.

“not disclosed” means the source does not publish the strength — it does not mean the product has none.

Australia ARTG data has no registration-status column, so status is shown as unknown; being on the register does not mean currently marketed.

EU centralised authorisation (EMA) — Authorised at EU level — not a record of sale in any single country. The EU register carries no strength, dosage form or pack size.

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The same ingredient can carry completely different brand names in different countries, and the same name can point to a different ingredient. Listed by country — not interchangeable.

Discontinued, withdrawn or unverified-status products are hidden by default; Hong Kong and Australia records are shown as exceptions.