Active Ingredient: BUPRENORPHINE HYDROCHLORIDE
Proprietary Name: BUPRENORPHINE HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 0.3MG BASE/ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A078331
Product Number: 001
Approval Date: Mar 27, 2007
Applicant Holder Full Name: AMERICAN REGENT INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
