CEFIZOX
CEFIZOX
Discontinued
DIN Number
01919490
Drug Class
Human
Market Date
Dec 31, 1988
Company
HC
GlaxoSmithKline 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 Number01919490
AIG Number0120453001
Classification & Schedule
C
Drug Class
Human
S
Schedule
Prescription
A
ATC Code
J01DD07 CEFTIZOXIME
Product Specifications
Dosage FormPowder For Solution
Route of AdministrationIntravenous
,
Intramuscular
AHFS Classification08:12.06.12
Health Canada Classification
ACTIVE INGREDIENTS (1)
CEFTIZOXIME SODIUMActive
Strength: 1 G / VIAL
Monograph: CEFTIZOXIME SODIUM