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Ceretec 0.5 mg Powder For Solution is a Health Canada–registered radiopharmaceutical drug (DIN 02329034) held by Ge Healthcare Canada Inc, containing Exametazime. Health Canada lists its status as Marketed (status date 17 Jan 2019). Nexara Health has matched 15 registrations of Exametazime across 7 other regulated markets.

Health Canada registration

DIN02329034
Brand nameCeretec
Active ingredientExametazime
Strength0.5 mg
Dosage formPowder For Solution
RouteIntravenous
CompanyGe Healthcare Canada Inc
StatusMarketed — 17 Jan 2019
ClassRadiopharmaceutical
ATCV09HA02 TECHNETIUM (99m Tc) EXAMETAZIME LABELLED CELLS
AHFS36:68.00 ; 78:00.00
Regulator recordHealth Canada DPD entry · Product monograph

Exametazime registered in other markets

15 registrations of the same molecule in 7 national registries outside Canada. Each row is taken from the regulator's own published list; status is shown as the registry reports it.

CountryProductMarketing authorisation holderStrengthFormStatusRegistry
Czech RepublicBrain-Spect Kit—0,3MGRad KitRSUKL DLP
Czech RepublicExametazim Radiopharmacy Laboratorium—500MCGRad KitRSUKL DLP
Czech RepublicStabilised Ceretec—500MCGRad KitRSUKL DLP
DenmarkMedi-ExametazimRadiopharmacy Laboratory Ltd.500 mikrogramradiofarmaceutisk præparationssætDecentral procedureLaegemiddelstyrelsen
DenmarkStabilised CeretecGE Healthcare ASradiofarmaceutisk præparationssætNationalLaegemiddelstyrelsen
Hong KongCeretec For InjGe Medical Systems Hong Kong LimitedRegisteredDH Drug Office
IcelandCeretecIcepharma - óskráðstl0Lyfjastofnun lyfjaverdskra
IcelandCeretecIcepharma - óskráðstl0Lyfjastofnun lyfjaverdskra
MaltaCeretec - Kit for the preparation of Technetium [99mTc] Exametazime InjectionGE Healthcare ASPowder For Solution For InjectionWithdrawnMedicines Authority
NetherlandsCeretec 0,5 mg kit voor radiofarmaceutische preparaatGE Healthcare B.V.Kit voor radiofarmaceutisch preparaatUitsluitend receptEU national register
NetherlandsExametazime Radiopharmacy 0,5 mg kit voor radiofarmaceutisch preparaatRadiopharmacy Laboratory LtdKit voor radiofarmaceutisch preparaatUitsluitend receptEU national register
NetherlandsStabilised Ceretec, 0,5 mg kit voor radiofarmaceutisch preparaatGE Healthcare B.V.Kit voor radiofarmaceutisch preparaatUitsluitend receptEU national register
TaiwanCeretecGe Healthcare Limited凍晶注射劑已註銷TFDA
TaiwanIner Hmpao Kit國家原子能科技研究院核醫製藥中心凍晶注射劑RegisteredTFDA
TaiwanMedi-Exametazime 500 micrograms Kit for radiopharmaceutical preparationMedi-Radiopharma Ltd.凍晶注射劑RegisteredTFDA

See every manufacturer of Exametazime worldwide →

Regulator price references for Exametazime

Published list or reimbursement prices for Exametazime presentations, in local currency, as at the date each registry last published. These are public reference prices, not Nexara Health quotes; strength and pack differ by row.

CountryProductStrengthPackPriceTypeSourceAs of
IcelandCeretechgl49,628.00 ISKmax wholesaleLyfjastofnun lyfjaverdskra2026-09-02
IcelandCeretechgl141,794.00 ISKmax wholesaleLyfjastofnun lyfjaverdskra2026-09-02

Marketed Canadian products with the same active ingredient

DINProductCompanyStrengthForm
02484048CeretecGe Healthcare Canada Inc0.5 mgKit ; Powder For Solution

Sourcing through Nexara Health

Nexara Health is a Health Canada–licensed wholesaler (DEL #3-002896) in Winnipeg. Because this DIN is marketed in Canada, supply normally comes through the Canadian channel; where the Canadian presentation is short or discontinued, the registrations above show which regulated markets hold an equivalent that can be imported under the Special Access Programme or for clinical comparator use. Request a quote or read how named-patient and foreign-pack supply works in Canada.

Frequently asked questions

Is Ceretec (DIN 02329034) marketed in Canada?

Yes. Health Canada lists DIN 02329034 as Marketed as of 17 Jan 2019.

Who holds the Canadian licence for this product?

Ge Healthcare Canada Inc is the company of record in the Health Canada Drug Product Database.

Is Exametazime registered outside Canada?

Yes — Nexara Health has matched 15 registrations in 7 other markets (see the table above).

Where does this data come from?

Health Canada Drug Product Database (DPD), DIN 02329034, status date 2019-01-17; national medicine registries: DH Drug Office, EU national register, Laegemiddelstyrelsen, Lyfjastofnun lyfjaverdskra, Medicines Authority, SUKL DLP, TFDA; price sources: Lyfjastofnun lyfjaverdskra. Nexara Health re-checks these sources weekly and shows the last verification date at the top of the page.

Source: Health Canada Drug Product Database (DPD), DIN 02329034, status date 2019-01-17; national medicine registries: DH Drug Office, EU national register, Laegemiddelstyrelsen, Lyfjastofnun lyfjaverdskra, Medicines Authority, SUKL DLP, TFDA; price sources: Lyfjastofnun lyfjaverdskra.

Health Canada Drug Product Database (DPD), DIN 02329034, status date 2019-01-17; national medicine registries: DH Drug Office, EU national register, Laegemiddelstyrelsen, Lyfjastofnun lyfjaverdskra, Medicines Authority, SUKL DLP, TFDA; price sources: Lyfjastofnun lyfjaverdskra. Last reviewed 2026-09-16. Nexara Health is a licensed wholesaler and supplies licensed entities only; consumer orders are routed to a partner pharmacy.