ApprovalTrail

Drug · DIN 01975501

EXPANDED MULTI-MED KIT

No: no longer authorized

The company stopped selling it and its DIN was cancelled. A cancellation is most often a business decision; the record does not say why.

Status Cancelled Post Market since February 28, 2005; first marketed December 31, 1992.
Drug Identification Number (DIN)
01975501
Company (DIN owner)
Edwards Lifesciences (Canada) Inc.Mississauga, Ontario, Canada
Schedule
Ethical
Dosage form
Kit; Ointment; Solution
Route
Topical; Intravenous; Block/Infiltration
Therapeutic class (ATC)
Lidocaine, combinations N01BB52
Class
Human
Record last updated
March 22, 2025

Active ingredients

As listed in the Drug Product Database.

IngredientStrengthPer
LIDOCAINE HYDROCHLORIDE1 %
POVIDONE-IODINE10 %
POVIDONE-IODINE10 %