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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: A074415
Product Number: 001
Approval Date: Jun 8, 1998
Applicant Holder Full Name: NOSTRUM LABORATORIES INC
Marketing Status:
Prescription
Patent and Exclusivity Information
