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Active Ingredient: AMIKACIN SULFATE
Proprietary Name: AMIKACIN SULFATE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 250MG BASE/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A205604
Product Number: 001
Approval Date: Dec 9, 2015
Applicant Holder Full Name: FRESENIUS KABI USA LLC
Marketing Status:
Prescription
Patent and Exclusivity Information
