NDC 72205-233 – Famotidine

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

Human Prescription Drug

Product NDC72205-233

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Novadoz Pharmaceuticals LLC
Dosage form
Powder, For Suspension
Route
Oral
Marketing category
ANDA · ANDA219863
Marketed since
July 24, 2025
Listing expires
December 31, 2026
Pharmacologic class
Histamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Famotidine →

Package NDC codes (1)

Package NDCDescriptionSince
72205-233-8455 mL in 1 BOTTLE (72205-233-84)Aug 16, 2025

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