BLOOD PACK UNIT CPD
BLOOD PACK UNIT CPD
Discontinued
DIN Number
00273953
Drug Class
Human
Market Date
Dec 31, 1969
Company
HC
fenwal labs, division of baxter corporation
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 Number00273953
AIG Number0409088001
Classification & Schedule
C
Drug Class
Human
S
Schedule
Ethical
A
ATC Code
V07AC BLOOD TRANSFUSION, AUXILIARY PRODUCTS
Product Specifications
Dosage FormBlood Collection
Route of AdministrationIntravenous
AHFS Classification20:12.04.92
Health Canada Classification
ACTIVE INGREDIENTS (4)
CITRIC ACIDActive
Strength: .327 %
Monograph: CITRIC ACID
DEXTROSEActive
Strength: 2.55 %
Monograph: DEXTROSE
SODIUM CITRATEActive
Strength: 2.63 %
Monograph: SODIUM CITRATE
SODIUM PHOSPHATE MONOBASICActive
Strength: .222 %
Monograph: SODIUM PHOSPHATE MONOBASIC