ApprovalTrail

Drug · DIN 02421135

CPD SOLUTION

USED AS A COMPONENT OF A MEDICAL DEVICE (BLOOD COLLECTION SETS)

No: cancelled before it was sold

Authorized, then cancelled before it was ever sold in Canada.

Status Cancelled Pre Market since June 26, 2022.
Drug Identification Number (DIN)
02421135
Company (DIN owner)
Laboratorios Grifols S.A.Parets Del Valles, Barcelona, Spain
Schedule
Ethical
Dosage form
Solution
Route
0-Unassigned
Therapeutic class (ATC)
Blood tests, auxiliary products V07AD
Class
Human
Record last updated
August 14, 2026

Active ingredients

As listed in the Drug Product Database.

IngredientStrengthPer
CITRIC ACID MONOHYDRATE0.327 G100 ML
SODIUM CITRATE DIHYDRATE2.63 G100 ML
SODIUM PHOSPHATE MONOBASIC, MONOHYDRATE0.222 G100 ML
DEXTROSE ANHYDROUS2.32 G100 ML