OPTIRAY 240 (ULTRAJECT)
OPTIRAY 240 (ULTRAJECT)
Discontinued
DIN Number
02035332
Drug Class
Human
Market Date
Dec 31, 1996
Company
HC
LIEBEL-FLARSHEIM COMPANY LLC
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 Number02035332
AIG Number0131317002
Classification & Schedule
C
Drug Class
Human
S
Schedule
Ethical
A
ATC Code
V08AB07 IOVERSOL
Product Specifications
Dosage FormSolution
Route of AdministrationSubarachnoidal
,
Intravascular
AHFS Classification36:68.00
Health Canada Classification
ACTIVE INGREDIENTS (1)
IOVERSOLActive
Strength: 51 % / W/V
Monograph: IOVERSOL