BRIETAL SODIUM AMPOULE 660
BRIETAL SODIUM AMPOULE 660
Discontinued
DIN Number
00128678
Drug Class
Human
Market Date
Dec 31, 1960
Company
HC
eli lilly 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 Number00128678
AIG Number0106022001
Classification & Schedule
C
Drug Class
Human
S
Schedule
Schedule G (CDSA IV)
A
ATC Code
N01AF01 METHOHEXITAL
Product Specifications
Dosage FormPowder For Solution
Route of AdministrationIntravenous
AHFS Classification28:24.04
Health Canada Classification
ACTIVE INGREDIENTS (1)
METHOHEXITAL SODIUMActive
Strength: 500 MG / AMP
Monograph: METHOHEXITAL SODIUM