Active Ingredient: GONADORELIN ACETATE
Proprietary Name: LUTREPULSE KIT
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 0.8MG/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N019687
Product Number: 001
Approval Date: Oct 10, 1989
Applicant Holder Full Name: FERRING PHARMACEUTICALS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
