DESFERAL 500MG
DESFERAL 500MG
Approved
DIN Number
01981242
Drug Class
Human
Market Date
Dec 31, 1992
Company
HC
novartis pharmaceuticals canada inc
Product Information
Detailed information about this Health Canada approved drug product, including dosage form, route of administration, and regulatory classification.
Product Details
Health Canada regulatory and product classification information
Regulatory Identifiers
DIN Number01981242
AIG Number0109208002
Classification & Schedule
C
Drug Class
Human
S
Schedule
Prescription
A
ATC Code
V03AC01 DEFEROXAMINE
Product Specifications
Dosage FormPowder For Solution
Route of AdministrationIntramuscular
,
Intravenous
,
Intraperitoneal
,
Subcutaneous
AHFS Classification64:00.00
Health Canada Classification
ACTIVE INGREDIENTS (1)
DEFEROXAMINE MESYLATEActive
Strength: 500 MG / VIAL
Monograph: DEFEROXAMINE MESYLATE