Strength
20 mg/1
Manufacturer
Rising Pharma Holdings Inc.NDC
64980062310
Classification
Generic
Dosage Form
TABLET, FILM COATED
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
FAMOTIDINEApproval Type
Generic (ANDA)
FDA Application
ANDA218181On Market Since
5/6/2024
Pharmacological Classes
Histamine H2 Receptor Antagonists
Histamine-2 Receptor Antagonist
FAMOTIDINE 20 MG TABLET
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