NDC 0832-6045 – Famotidine

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

Human Prescription Drug

Product NDC0832-6045

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Upsher-Smith Laboratories, LLC
Dosage form
Powder, For Suspension
Route
Oral
Marketing category
ANDA · ANDA217655
Marketed since
June 16, 2023
Listing expires
December 31, 2026
Pharmacologic class
Histamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Famotidine →

Package NDC codes (3)

Package NDCDescriptionSince
0832-6045-10100 mL in 1 BOTTLE (0832-6045-10)Oct 27, 2023
0832-6045-15150 mL in 1 BOTTLE (0832-6045-15)Oct 27, 2023
0832-6045-5050 mL in 1 BOTTLE (0832-6045-50)Jul 11, 2023

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