Active Ingredient: LEUPROLIDE ACETATE
Proprietary Name: VIADUR
Dosage Form; Route of Administration: IMPLANT; IMPLANTATION
Strength: EQ 65MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N021088
Product Number: 001
Approval Date: Mar 3, 2000
Applicant Holder Full Name: ORTHO MCNEIL JANSSEN PHARMACEUTICAL INC
Marketing Status:
Discontinued
Patent and Exclusivity Information