SANDOZ OPTICORT
SANDOZ OPTICORT
Discontinued
DIN Number
02247920
Drug Class
Human
Market Date
Jan 16, 2004
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 Number02247920
AIG Number0305701001
Classification & Schedule
C
Drug Class
Human
S
Schedule
Prescription
A
ATC Code
S03CA01 DEXAMETHASONE AND ANTIINFECTIVES
Product Specifications
Dosage FormSolution
Route of AdministrationOtic
,
Ophthalmic
AHFS Classification52:04.04
Health Canada Classification
ACTIVE INGREDIENTS (3)
DEXAMETHASONE (DEXAMETHASONE SODIUM METASULPHOBENZOATE)Active
Strength: 0.5 MG / ML
Monograph: DEXAMETHASONE (DEXAMETHASONE SODIUM METASULPHOBENZOATE)
FRAMYCETIN SULFATEActive
Strength: 5 MG / ML
Monograph: FRAMYCETIN SULFATE
GRAMICIDINActive
Strength: 0.05 MG / ML
Monograph: GRAMICIDIN