FERTINORM HP 75 - PWS DILUENT IM SC
FERTINORM HP 75 - PWS DILUENT IM SC
Discontinued
DIN Number
02125404
Drug Class
Human
Market Date
Dec 31, 1994
Company
HC
emd serono, a division of emd inc., canada
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 Number02125404
AIG Number0226677001
Classification & Schedule
C
Drug Class
Human
S
Schedule
Schedule D
,
Prescription
A
ATC Code
G03GA04 UROFOLLITROPIN
Product Specifications
Dosage FormPowder For Solution
,
Liquid
Route of AdministrationSubcutaneous
,
Intramuscular
AHFS Classification68:18.00
Health Canada Classification
ACTIVE INGREDIENTS (2)
SODIUM CHLORIDEActive
Strength: 2 ML / KIT
Monograph: SODIUM CHLORIDE
UROFOLLITROPINActive
Strength: 75 UNIT / KIT
Monograph: UROFOLLITROPIN