MedPath

PRIMAXIN 500

PRIMAXIN 500

Discontinued
DIN Number

00717282

Drug Class

Human

Market Date

Dec 31, 1987

Company
HC

Merck 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 Number00717282
AIG Number0218820001
Classification & Schedule
C
Drug Class
Human
S
Schedule
Prescription
A
ATC Code
J01DH51 IMIPENEM AND CILASTATIN
Product Specifications
Dosage FormPowder For Solution
Route of AdministrationIntravenous
AHFS Classification08:12.07.08
Health Canada Classification

ACTIVE INGREDIENTS (2)

CILASTATIN (CILASTATIN SODIUM)Active
Strength: 500 MG / VIAL
Monograph: CILASTATIN (CILASTATIN SODIUM)
IMIPENEMActive
Strength: 500 MG / VIAL
Monograph: IMIPENEM

MedPath

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

© 2025 MedPath, Inc. All rights reserved.