NDC 67877-775 – Famotidine

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

Human Prescription Drug

Product NDC67877-775

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Ascend Laboratories, LLC
Dosage form
Powder, For Suspension
Route
Oral
Marketing category
ANDA · ANDA216400
Marketed since
August 24, 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
67877-775-8950 mL in 1 BOTTLE (67877-775-89)Aug 24, 2023

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