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Credelio Plus 56.25 mg Tablet (Chewable) is a Health Canada–registered veterinary drug (DIN 02525674) held by Elanco Canada Limited, containing Lotilaner. Health Canada lists its status as Marketed (status date 04 Aug 2022). Nexara Health has matched 53 registrations of Lotilaner across 5 other regulated markets, 1 of them in the same strength and dosage form.

Health Canada registration

DIN02525674
Brand nameCredelio Plus
Active ingredientLotilaner
Strength56.25 mg
Dosage formTablet (Chewable)
RouteOral
CompanyElanco Canada Limited
StatusMarketed — 04 Aug 2022
ClassVeterinary
ATC
AHFS
Regulator recordHealth Canada DPD entry · Product monograph

Lotilaner registered in other markets

53 registrations of the same molecule in 5 national registries outside Canada (first 30 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
PolandCredelio 900 mgElanco GmbH900 mgTabletka do rozgryzania i żuciaURPL RPL
DenmarkAdTab til hunde >11-22 kgElanco GmbH450 mgtyggetabletterCentralLaegemiddelstyrelsen
DenmarkAdTab til hunde >2.5-5.5 kgElanco GmbH112 mgtyggetabletterCentralLaegemiddelstyrelsen
DenmarkAdTab til hunde >22-45 kgElanco GmbH900 mgtyggetabletterCentralLaegemiddelstyrelsen
DenmarkAdTab til hunde >5.5-11 kgElanco GmbH225 mgtyggetabletterCentralLaegemiddelstyrelsen
DenmarkAdTab til hunde 1.3-2.5 kgElanco GmbH56 mgtyggetabletterCentralLaegemiddelstyrelsen
DenmarkAdTab til katte >2.0-8.0 kgElanco GmbH48 mgtyggetabletterCentralLaegemiddelstyrelsen
DenmarkAdTab til katte 0.5-2.0 kgElanco GmbH12 mgtyggetabletterCentralLaegemiddelstyrelsen
DenmarkCredelioElanco GmbH56 mgtyggetabletterCentralLaegemiddelstyrelsen
European Union (EMA)AdTab (previously Lotilaner Elanco)—AuthorisedEMA centrally authorised
European Union (EMA)Credelio—AuthorisedEMA centrally authorised
European Union (EMA)Lotimax—AuthorisedEMA centrally authorised
FinlandAdTabElanco GmbH225 mgpurutablettiMyyntilupa myönnettyFimea Perusrekisteri
FinlandAdTabElanco GmbH900 mgpurutablettiMyyntilupa myönnettyFimea Perusrekisteri
FinlandAdTabElanco GmbH112 mgpurutablettiMyyntilupa myönnettyFimea Perusrekisteri
FinlandAdTabElanco GmbH56 mgpurutablettiMyyntilupa myönnettyFimea Perusrekisteri
FinlandAdTabElanco GmbH450 mgpurutablettiMyyntilupa myönnettyFimea Perusrekisteri
FinlandAdTabElanco GmbH12 mgpurutablettiMyyntilupa myönnettyFimea Perusrekisteri
FinlandAdTabElanco GmbH48 mgpurutablettiMyyntilupa myönnettyFimea Perusrekisteri
FinlandCredelioElanco GmbH48 mgpurutablettiMyyntilupa myönnettyFimea Perusrekisteri
PolandAdTabElanco GmbH900 mgTabletka do rozgryzania i żuciaURPL RPL
PolandLotimaxElanco GmbH450 mgTabletka do rozgryzania i żuciaBezterminoweURPL RPL
United StateslotilanerElanco US Inc.Tablet, ChewableFDA NDC
United StateslotilanerElanco US Inc.Tablet, ChewableFDA NDC
United StateslotilanerElanco US Inc.Tablet, ChewableFDA NDC
United StateslotilanerElanco US Inc.Tablet, ChewableFDA NDC
United StateslotilanerElanco US Inc.Tablet, ChewableFDA NDC
United StateslotilanerElanco US Inc.Tablet, ChewableFDA NDC
United StateslotilanerElanco US Inc.Tablet, ChewableFDA NDC
United StatesLotilanerPROCOS SpAPowderFDA NDC

See every manufacturer of Lotilaner 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 Credelio Plus (DIN 02525674) marketed in Canada?

Yes. Health Canada lists DIN 02525674 as Marketed as of 04 Aug 2022.

Who holds the Canadian licence for this product?

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

Is Lotilaner registered outside Canada?

Yes — Nexara Health has matched 53 registrations in 5 other markets, including 1 in the same strength and dosage form (see the table above).

Where does this data come from?

Health Canada Drug Product Database (DPD), DIN 02525674, status date 2022-08-04; national medicine registries: EMA centrally authorised, FDA NDC, Fimea Perusrekisteri, Laegemiddelstyrelsen, 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 02525674, status date 2022-08-04; national medicine registries: EMA centrally authorised, FDA NDC, Fimea Perusrekisteri, Laegemiddelstyrelsen, URPL RPL.

Health Canada Drug Product Database (DPD), DIN 02525674, status date 2022-08-04; national medicine registries: EMA centrally authorised, FDA NDC, Fimea Perusrekisteri, Laegemiddelstyrelsen, 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.