Active Ingredient: POTASSIUM CHLORIDE
Proprietary Name: POTASSIUM CHLORIDE
Dosage Form; Route of Administration: FOR SOLUTION; ORAL
Strength: 20MEQ
Reference Listed Drug: No
Reference Standard: No
TE Code: AA
Application Number: A210902
Product Number: 001
Approval Date: May 23, 2019
Applicant Holder Full Name: AMNEAL PHARMACEUTICALS LLC
Marketing Status:
Prescription
Patent and Exclusivity Information
