IFEX PWS 2G/VIAL
IFEX PWS 2G/VIAL
Discontinued
DIN Number
00797235
Drug Class
Human
Market Date
Dec 31, 1989
Company
HC
bristol labs division of bristol-myers squibb
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 Number00797235
AIG Number0120706003
Classification & Schedule
C
Drug Class
Human
S
Schedule
Prescription
A
ATC Code
L01AA06 IFOSFAMIDE
Product Specifications
Dosage FormPowder For Solution
Route of AdministrationIntravenous
AHFS Classification10:00.00
Health Canada Classification
ACTIVE INGREDIENTS (1)
IFOSFAMIDEActive
Strength: 2 G / VIAL
Monograph: IFOSFAMIDE