Active Ingredient: BUPRENORPHINE HYDROCHLORIDE
Proprietary Name: PROBUPHINE
Dosage Form; Route of Administration: IMPLANT; IMPLANTATION
Strength: EQ 80MG BASE/IMPLANT
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N204442
Product Number: 001
Approval Date: May 26, 2016
Applicant Holder Full Name: REACX PHARMACEUTICALS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
