U.S. flag An official website of the United States government
  1. Home
  2. Drug Databases
  3. Orange Book Home

Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

Home | Back to Search Results

Product Details for ANDA 211884

SUCRALFATE (SUCRALFATE)
1GM/10ML
Marketing Status: Prescription
Active Ingredient: SUCRALFATE
Proprietary Name: SUCRALFATE
Dosage Form; Route of Administration: SUSPENSION; ORAL
Strength: 1GM/10ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A211884
Product Number: 001
Approval Date: Mar 15, 2022
Applicant Holder Full Name: VISTAPHARM INC
Marketing Status:  Prescription
Patent and Exclusivity Information
Back to Top