CEFIZOX
CEFIZOX
Discontinued
DIN Number
01919504
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 Number01919504
AIG Number0120453003
Classification & Schedule
C
Drug Class
Human
S
Schedule
Prescription
A
ATC Code
J01DD07 CEFTIZOXIME
Product Specifications
Dosage FormPowder For Solution
Route of AdministrationIntramuscular
,
Intravenous
AHFS Classification08:12.06.12
Health Canada Classification
ACTIVE INGREDIENTS (1)
CEFTIZOXIME SODIUMActive
Strength: 2 G
Monograph: CEFTIZOXIME SODIUM