Strength
40 mg/5mL
Manufacturer
Camber Pharmaceuticals Inc.NDC
31722006331
Classification
Generic
Dosage Form
POWDER, FOR SUSPENSION
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
FAMOTIDINEApproval Type
Generic (ANDA)
FDA Application
ANDA217330On Market Since
8/17/2023
Pharmacological Classes
Histamine H2 Receptor Antagonists
Histamine-2 Receptor Antagonist
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