Active Ingredient: POTASSIUM CHLORIDE
Proprietary Name: SLOW-K
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 8MEQ
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N017476
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: NOVARTIS PHARMACEUTICALS CORP
Marketing Status:
Discontinued
Patent and Exclusivity Information
