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Active Ingredient: ZOLEDRONIC ACID
Proprietary Name: ZOLEDRONIC ACID
Dosage Form; Route of Administration: INJECTABLE; INTRAVENOUS
Strength: EQ 4MG BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: Application Number: A090018
Product Number: 001
Approval Date: Mar 4, 2013
Applicant Holder Full Name: SUN PHARMA GLOBAL FZE
Marketing Status:
Discontinued
Patent and Exclusivity Information
