NDC 60219-2090 – Famotidine

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

Human Prescription Drug

Product NDC60219-2090

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Amneal Pharmaceuticals NY LLC
Dosage form
Powder, For Suspension
Route
Oral
Marketing category
ANDA · ANDA216427
Marketed since
May 13, 2024
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
60219-2090-450 mL in 1 BOTTLE (60219-2090-4)May 13, 2024

Other Famotidine products