ZINACEF INJECTION - PWS IM IV 750MG/VIAL
ZINACEF INJECTION - PWS IM IV 750MG/VIAL
Discontinued
DIN Number
02213532
Drug Class
Human
Market Date
Aug 20, 2001
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 Number02213532
AIG Number0113736002
Classification & Schedule
C
Drug Class
Human
S
Schedule
Prescription
A
ATC Code
J01DC02 CEFUROXIME
Product Specifications
Dosage FormPowder For Solution
Route of AdministrationIntravenous
,
Intramuscular
AHFS Classification08:12.06.08
Health Canada Classification
ACTIVE INGREDIENTS (1)
CEFUROXIME SODIUMActive
Strength: 750 MG / VIAL
Monograph: CEFUROXIME SODIUM