Active Ingredient: IBANDRONATE SODIUM
Proprietary Name: IBANDRONATE SODIUM
Dosage Form; Route of Administration: INJECTABLE; INTRAVENOUS
Strength: EQ 3MG BASE/3ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A090853
Product Number: 001
Approval Date: Feb 14, 2014
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status:
Prescription
Patent and Exclusivity Information