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Active Ingredient: ZOLEDRONIC ACID
Proprietary Name: ZOLEDRONIC ACID
Dosage Form; Route of Administration: INJECTABLE; INTRAVENOUS
Strength: EQ 4MG BASE/5ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A202182
Product Number: 001
Approval Date: Jun 3, 2013
Applicant Holder Full Name: HIKMA FARMACEUTICA SA
Marketing Status:
Prescription
Patent and Exclusivity Information