Active Ingredient: AMIKACIN SULFATE
Proprietary Name: AMIKACIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 500MG BASE/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A064146
Product Number: 001
Approval Date: Apr 2, 1997
Applicant Holder Full Name: HOSPIRA WORLDWIDE, INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
