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Active Ingredient: SODIUM ACETATE
Proprietary Name: SODIUM ACETATE
Dosage Form; Route of Administration: SOLUTION; INTRAVENOUS
Strength: 400MEQ/100ML (4MEQ/ML)
Reference Listed Drug: No
Reference Standard: Yes
TE Code: AP
Application Number: A206687
Product Number: 001
Approval Date: Oct 30, 2017
Applicant Holder Full Name: FRESENIUS KABI USA LLC
Marketing Status:
Prescription
Patent and Exclusivity Information
