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: A209314
Product Number: 002
Approval Date: Jun 22, 2018
Applicant Holder Full Name: YICHANG HUMANWELL PHARMACEUTICAL CO LTD
Marketing Status:
Prescription
Patent and Exclusivity Information