NDC 0517-9302 – Multrys

Zinc Sulfate 2470 ug/mL; Cupric Sulfate 150 ug/mL; Manganese Sulfate 8.22 ug/mL; Selenious Acid 9.8 ug/mL · Injection, Solution · Intravenous

Human Prescription Drug 1 recall

Product NDC0517-9302

Product details

Brand name
Multrys
Generic name
Trace Elements Injection 4
Labeler
American Regent, Inc.
Dosage form
Injection, Solution
Route
Intravenous
Marketing category
NDA · NDA209376
Marketed since
September 1, 2021
Listing expires
December 31, 2026
Pharmacologic class
Copper Absorption Inhibitor; Paramagnetic Contrast Agent

Active ingredients

Uses, dosage, side effects and warnings for Multrys →

Package NDC codes (1)

Package NDCDescriptionSince
0517-9302-2525 VIAL, SINGLE-DOSE in 1 TRAY (0517-9302-25) / 1 mL in 1 VIAL, SINGLE-DOSE (0517-9302-01)Sep 1, 2021

Recalls mentioning this NDC