NDC 0641-6023 – Famotidine

Famotidine 10 mg/mL · Injection · Intravenous

Human Prescription Drug

Product NDC0641-6023

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
Injection
Route
Intravenous
Marketing category
ANDA · ANDA075488
Marketed since
April 16, 2001
Listing expires
December 31, 2026
Pharmacologic class
Histamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Famotidine →

Package NDC codes (2)

Package NDCDescriptionSince
0641-6023-1010 VIAL in 1 CARTON (0641-6023-10) / 4 mL in 1 VIAL (0641-6023-01)May 16, 2023
0641-6023-2525 VIAL in 1 CARTON (0641-6023-25) / 4 mL in 1 VIAL (0641-6023-01)Apr 16, 2001

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