MedPath

PHENYTOIN SODIUM INJECTION USP

PHENYTOIN SODIUM INJECTION USP

Approved
DIN Number

00780626

Drug Class

Human

Market Date

Dec 31, 1988

Company
HC

Sandoz Canada, 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 Number00780626
AIG Number0101375003
Classification & Schedule
C
Drug Class
Human
S
Schedule
Prescription
A
ATC Code
N03AB02 PHENYTOIN
Product Specifications
Dosage FormLiquid
Route of AdministrationIntramuscular ,  Intravenous
AHFS Classification28:12.12
Health Canada Classification

ACTIVE INGREDIENTS (1)

PHENYTOIN SODIUMActive
Strength: 50 MG / ML
Monograph: PHENYTOIN SODIUM

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.