LUTREPULSE
LUTREPULSE
Dormant
DIN Number
02046202
Drug Class
Human
Market Date
Dec 31, 1994
Company
HC
Ferring 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 Number02046202
AIG Number0121867001
Classification & Schedule
C
Drug Class
Human
S
Schedule
Prescription
A
ATC Code
H01CA01 GONADORELIN
Product Specifications
Dosage FormPowder For Solution
Route of AdministrationIntravenous
,
Subcutaneous
AHFS Classification68:18.00
Health Canada Classification
ACTIVE INGREDIENTS (1)
GONADORELIN ACETATEActive
Strength: 3.2 MG / VIAL
Monograph: GONADORELIN ACETATE