NDC 63323-738 – Famotidine

Famotidine 10 mg/mL · Injection, Solution · Intravenous

Human Prescription Drug

Product NDC63323-738

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Fresenius Kabi USA, LLC
Dosage form
Injection, Solution
Route
Intravenous
Marketing category
ANDA · ANDA075709
Marketed since
July 19, 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
63323-738-0910 VIAL, MULTI-DOSE in 1 TRAY (63323-738-09) / 4 mL in 1 VIAL, MULTI-DOSE (63323-738-03)Jul 19, 2001
63323-738-2010 VIAL, MULTI-DOSE in 1 TRAY (63323-738-20) / 20 mL in 1 VIAL, MULTI-DOSE (63323-738-06)Jul 19, 2001

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