NDC 81033-023 – Famotidine

Famotidine 40 mg/5mL · Powder, For Suspension · Oral

Human Prescription Drug

Product NDC81033-023

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Kesin Pharma Corporation
Dosage form
Powder, For Suspension
Route
Oral
Marketing category
ANDA · ANDA217137
Marketed since
August 10, 2023
Listing expires
December 31, 2027
Pharmacologic class
Histamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Famotidine →

Package NDC codes (1)

Package NDCDescriptionSince
81033-023-5050 mL in 1 BOTTLE (81033-023-50)Nov 25, 2025

Other Famotidine products