NDC 63323-010 – Gentamicin

Gentamicin Sulfate 40 mg/mL · Injection, Solution · Intramuscular, Intravenous

Human Prescription Drug 1 recall

Product NDC63323-010

Product details

Brand name
Gentamicin
Generic name
Gentamicin Sulfate
Labeler
Fresenius Kabi USA, LLC
Dosage form
Injection, Solution
Route
Intramuscular, Intravenous
Marketing category
ANDA · ANDA062366
Marketed since
August 10, 2000
Listing expires
December 31, 2026
Pharmacologic class
Aminoglycoside Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Gentamicin →

Package NDC codes (5)

Package NDCDescriptionSince
63323-010-0225 VIAL in 1 TRAY (63323-010-02) / 2 mL in 1 VIAL (63323-010-01)Aug 10, 2000
63323-010-2025 VIAL in 1 TRAY (63323-010-20) / 20 mL in 1 VIAL (63323-010-03)Aug 10, 2000
63323-010-9425 VIAL, MULTI-DOSE in 1 TRAY (63323-010-94) / 2 mL in 1 VIAL, MULTI-DOSE (63323-010-41)Aug 10, 2000
63323-010-9525 VIAL, MULTI-DOSE in 1 TRAY (63323-010-95) / 20 mL in 1 VIAL, MULTI-DOSE (63323-010-42)Aug 10, 2000
63323-010-9625 VIAL, MULTI-DOSE in 1 TRAY (63323-010-96) / 20 mL in 1 VIAL, MULTI-DOSEAug 10, 2000

Recalls mentioning this NDC

Other Gentamicin products