Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 50458-0543-60 recalled?

Invokamet · 60 TABLET, FILM COATED in 1 BOTTLE (50458-543-60)

Yes — this exact package was recalled

1 FDA recall names the code 50458-0543-60 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.

Active ingredient
canagliflozin and metformin hydrochloride
Strength
CANAGLIFLOZIN 150 mg/1; METFORMIN HYDROCHLORIDE 1000 mg/1
Form
Tablet, Film Coated · Oral
Labeler
Janssen Pharmaceuticals, Inc.
Type
Human Prescription Drug
Product code
50458-0543

Recalls naming this package

Class III ยท Low risk

Invokamet (canagliflozin and metformin HCl)

Labeling: Incorrect or Missing Package Insert - Xarelto prescribing information outserts may be affixed to the exterior of Invokamet bottles in place of the Invokamet prescribing information outsert.

Terminated Labeling / mix-up Janssen Ortho L.L.C. NDC 50458-543-60 D-0115-2017

Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.

Other recalled products from this labeler