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Active Ingredient: POTASSIUM CHLORIDE
Proprietary Name: POTASSIUM CHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 2MEQ/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: Application Number: A087817
Product Number: 001
Approval Date: Oct 20, 1982
Applicant Holder Full Name: FRESENIUS KABI USA LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information
