Active Ingredient: CHOLESTYRAMINE
Proprietary Name: LOCHOLEST LIGHT
Dosage Form; Route of Administration: POWDER; ORAL
Strength: EQ 4GM RESIN/SCOOPFUL
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A074562
Product Number: 002
Approval Date: Aug 15, 1996
Applicant Holder Full Name: CHARTWELL RX SCIENCES LLC
Marketing Status:
Prescription
Patent and Exclusivity Information