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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 019183

CARAFATE (SUCRALFATE)
1GM/10ML
Marketing Status: Prescription
Active Ingredient: SUCRALFATE
Proprietary Name: CARAFATE
Dosage Form; Route of Administration: SUSPENSION; ORAL
Strength: 1GM/10ML
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AB
Application Number: N019183
Product Number: 001
Approval Date: Dec 16, 1993
Applicant Holder Full Name: ABBVIE INC
Marketing Status:  Prescription
Patent and Exclusivity Information
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