Active Ingredient: BUPRENORPHINE HYDROCHLORIDE
Proprietary Name: BUPRENORPHINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; SUBLINGUAL
Strength: EQ 2MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A090360
Product Number: 001
Approval Date: May 7, 2010
Applicant Holder Full Name: BARR LABORATORIES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information