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Component Te-S Implants With Tylan 29 mg Implant is a Health Canada–registered veterinary drug (DIN 02245745) held by Elanco Canada Limited, containing Tylosin Tartrate. Health Canada lists its status as Marketed (status date 13 Jan 2020). Nexara Health has matched 24 registrations of Tylosin Tartrate across 4 other regulated markets.

Health Canada registration

DIN02245745
Brand nameComponent Te-S Implants With Tylan
Active ingredientTylosin Tartrate
Strength29 mg
Dosage formImplant
RouteSubcutaneous
CompanyElanco Canada Limited
StatusMarketed — 13 Jan 2020
ClassVeterinary
ATC
AHFS
Regulator recordHealth Canada DPD entry · Product monograph

Tylosin Tartrate registered in other markets

24 registrations of the same molecule in 4 national registries outside Canada (first 21 shown, exact strength and form first). Each row is taken from the regulator's own published list; status is shown as the registry reports it.

CountryProductMarketing authorisation holderStrengthFormStatusRegistry
DenmarkTilsing Vet.Dopharma Research B.V.200.000 IE/mlinjektionsvæske, opløsningDecentral procedureLaegemiddelstyrelsen
DenmarkTylan Vet.Elanco GmbH200 mg/mlinjektionsvæske, opløsningNationalLaegemiddelstyrelsen
DenmarkTylmasinHuvepharma NV200 mg/mlinjektionsvæske, opløsningDecentral procedureLaegemiddelstyrelsen
DenmarkTylovetBiovet J.S.C.200 mg/mlinjektionsvæske, opløsningDecentral procedureLaegemiddelstyrelsen
DenmarkTylucylVetoquinol Scandinavia AB200 mg/mlinjektionsvæske, opløsningDecentral procedureLaegemiddelstyrelsen
MalaysiaINECTIL 20% Injectable solutionLaboratorios Reveex (asia) Sdn. Bhd.VeterinaryPRODUCT APPROVEDNPRA
MalaysiaTylan 200 mg/ml InjectionElanco Malaysia Sdn BhdVeterinaryPRODUCT APPROVEDNPRA
MalaysiaVime Tylovet 50 mg/ml Solution for InjectionVemedim Sdn BhdVeterinaryPRODUCT APPROVEDNPRA
PolandBiotyl 200Biowet Drwalew Sp. z o.o.20 g / 100 mlRoztwór do wstrzykiwańBezterminoweURPL RPL
PolandBiotyl 50Biowet Drwalew Sp. z o.o.5 g / 100 mlRoztwór do wstrzykiwańBezterminoweURPL RPL
PolandDophatyl-jectDopharma Research B.V.200000 j.m./mlRoztwór do wstrzykiwańBezterminoweURPL RPL
PolandPharmasinHuvepharma NV200 mg/mlRoztwór do wstrzykiwańBezterminoweURPL RPL
PolandPharmasinHuvepharma NV250 000 IUGranulat doustnyBezterminoweURPL RPL
PolandTilsolCeva Salute Animale S.p.A.200 g/1000 gProszek do sporządzania roztworu doustnegoBezterminoweURPL RPL
PolandTylan G 100 PremixElanco GmbH100 g/1 kgPremiks do sporządzania paszy leczniczejBezterminoweURPL RPL
PolandTylan Soluble PowderElanco GmbH1000 g/ 1 kgProszek do sporządzania roztworu doustnego2026-10-10URPL RPL
United StatestylosinShandong Lukang Shelile Pharmaceutical Co.,LtdPowderFDA NDC
United Statestylosin phosphateShandong Lukang Shelile Pharmaceutical Co.,LtdPowderFDA NDC
United StatesTylosin tartrateShandong Lukang Shelile Pharmaceutical Co., Ltd.PowderFDA NDC
United StatesTylosin TartrateNingxia Taiyicin Biotech Co., Ltd.PowderFDA NDC
United StatesTylosin TartrateMedisca Inc.PowderFDA NDC

See every manufacturer of Tylosin Tartrate worldwide →

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 Component Te-S Implants With Tylan (DIN 02245745) marketed in Canada?

Yes. Health Canada lists DIN 02245745 as Marketed as of 13 Jan 2020.

Who holds the Canadian licence for this product?

Elanco Canada Limited is the company of record in the Health Canada Drug Product Database.

Is Tylosin Tartrate registered outside Canada?

Yes — Nexara Health has matched 24 registrations in 4 other markets (see the table above).

Where does this data come from?

Health Canada Drug Product Database (DPD), DIN 02245745, status date 2020-01-13; national medicine registries: FDA NDC, Laegemiddelstyrelsen, NPRA, URPL RPL. 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 02245745, status date 2020-01-13; national medicine registries: FDA NDC, Laegemiddelstyrelsen, NPRA, URPL RPL.

Health Canada Drug Product Database (DPD), DIN 02245745, status date 2020-01-13; national medicine registries: FDA NDC, Laegemiddelstyrelsen, NPRA, URPL RPL. Last reviewed 2026-09-16. Nexara Health is a licensed wholesaler and supplies licensed entities only; consumer orders are routed to a partner pharmacy.