Active Ingredient: SUCRALFATE
Proprietary Name: SUCRALFATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 1GM
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A070848
Product Number: 001
Approval Date: Mar 29, 1996
Applicant Holder Full Name: TEVA PHARMACEUTICALS USA INC
Marketing Status:
Prescription
Patent and Exclusivity Information