XIGRIS (5MG/VIAL)
XIGRIS (5MG/VIAL)
Discontinued
DIN Number
02247129
Drug Class
Human
Market Date
Feb 20, 2003
Company
HC
eli lilly 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 Number02247129
AIG Number0148944001
Classification & Schedule
C
Drug Class
Human
S
Schedule
Prescription
,
Schedule D
A
ATC Code
B01AD10 DROTRECOGIN ALFA
Product Specifications
Dosage FormPowder For Solution
Route of AdministrationIntravenous
AHFS Classification92:92.00
Health Canada Classification
ACTIVE INGREDIENTS (1)
DROTRECOGIN ALFA (ACTIVATED)Active
Strength: 5 MG / VIAL
Monograph: DROTRECOGIN ALFA (ACTIVATED)