Active Ingredient: POTASSIUM CHLORIDE
Proprietary Name: POTASSIUM CHLORIDE
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 10MEQ
Reference Listed Drug: No
Reference Standard: No
TE Code: AB2
Application Number: A211797
Product Number: 002
Approval Date: Mar 4, 2020
Applicant Holder Full Name: GRANULES PHARMACEUTICALS INC
Marketing Status:
Prescription
Patent and Exclusivity Information
