PUREGON 100 I.U.
PUREGON 100 I.U.
Discontinued
DIN Number
02231656
Drug Class
Human
Market Date
Oct 8, 1997
Company
HC
organon canada ltd ltee
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 Number02231656
AIG Number0232900003
Classification & Schedule
C
Drug Class
Human
S
Schedule
Schedule D
,
Prescription
A
ATC Code
G03GA06 FOLLITROPIN BETA
Product Specifications
Dosage FormLiquid
,
Powder For Solution
Route of AdministrationSubcutaneous
,
Intramuscular
AHFS Classification68:18.00
Health Canada Classification
ACTIVE INGREDIENTS (2)
FOLLITROPIN BETAActive
Strength: 100 UNIT / KIT
Monograph: FOLLITROPIN BETA
SODIUM CHLORIDEActive
Strength: 1 ML / KIT
Monograph: SODIUM CHLORIDE