LMD 10% IN 0.9% SODIUM CHLORIDE
LMD 10% IN 0.9% SODIUM CHLORIDE
Approved
DIN Number
00224227
Drug Class
Human
Market Date
Dec 31, 1968
Company
HC
Pfizer Canada Ulc
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 Number00224227
AIG Number0200213001
Classification & Schedule
C
Drug Class
Human
S
Schedule
Ethical
A
ATC Code
B05AA55 DEXTRAN,COMBINATIONS
Product Specifications
Dosage FormSolution
Route of AdministrationIntravenous
AHFS Classification40:12.00
Health Canada Classification
ACTIVE INGREDIENTS (2)
DEXTRANActive
Strength: 10 %
Monograph: DEXTRAN
SODIUM CHLORIDEActive
Strength: 0.9 %
Monograph: SODIUM CHLORIDE