Strength
1 g/10mL
Manufacturer
Pacific Pharma, Inc.NDC
82182010614
Classification
Generic
Dosage Form
SUSPENSION
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
SUCRALFATEApproval Type
Authorized Generic (NDA)
FDA Application
NDA019183On Market Since
2/1/2024
Pharmacological Classes
Aluminum Complex
Organometallic Compounds
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