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: AB1
Application Number: A075604
Product Number: 001
Approval Date: Apr 10, 2002
Applicant Holder Full Name: ACTAVIS LABORATORIES FL INC
Marketing Status:
Prescription
Patent and Exclusivity Information