Strength
1 g/1
Manufacturer
Teva Pharmaceuticals USA Inc.NDC
00093221098
Classification
Generic
Dosage Form
TABLET
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
SUCRALFATEApproval Type
Generic (ANDA)
FDA Application
ANDA070848On Market Since
11/11/1996
Pharmacological Classes
Aluminum Complex
Organometallic Compounds
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