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: AP
Application Number: A076931
Product Number: 001
Approval Date: Mar 2, 2005
Applicant Holder Full Name: HIKMA PHARMACEUTICALS USA INC
Marketing Status:
Prescription
Patent and Exclusivity Information
