IBUPROFEN TABLETS
IBUPROFEN TABLETS
Dormant
DIN Number
02368072
Drug Class
Human
Market Date
Jan 26, 2017
Company
HC
vita health products 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 Number02368072
AIG Number0108883004
Classification & Schedule
C
Drug Class
Human
S
Schedule
OTC
A
ATC Code
M01AE01 IBUPROFEN
Product Specifications
Dosage FormTablet
Route of AdministrationOral
AHFS Classification28:08.04.92
Health Canada Classification
ACTIVE INGREDIENTS (1)
IBUPROFENActive
Strength: 200 MG
Monograph: IBUPROFEN