IBUPROFEN NIGHTTIME
IBUPROFEN NIGHTTIME
Dormant
DIN Number
02430770
Drug Class
Human
Market Date
Jan 27, 2015
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 Number02430770
AIG Number0252788001
Classification & Schedule
C
Drug Class
Human
S
Schedule
OTC
A
ATC Code
M01AE51 IBUPROFEN, COMBINATIONS
Product Specifications
Dosage FormCapsule
Route of AdministrationOral
AHFS Classification04:04.04
Health Canada Classification
ACTIVE INGREDIENTS (2)
DIPHENHYDRAMINE HYDROCHLORIDEActive
Strength: 25 MG
Monograph: DIPHENHYDRAMINE HYDROCHLORIDE
IBUPROFENActive
Strength: 200 MG
Monograph: IBUPROFEN