Strength
1 g/1
Manufacturer
Greenstone LLCNDC
59762040105
Classification
Generic
Dosage Form
TABLET
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
SUCRALFATEApproval Type
Authorized Generic (NDA)
FDA Application
NDA018333On Market Since
9/25/2017
Pharmacological Classes
Aluminum Complex
Organometallic Compounds
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