NDC 0517-6502 – Selenious Acid

Selenium 6 ug/mL · Injection, Solution · Intravenous

Human Prescription Drug 1 recall

Product NDC0517-6502

Product details

Brand name
Selenious Acid
Generic name
Selenious Acid
Labeler
American Regent, Inc.
Dosage form
Injection, Solution
Route
Intravenous
Marketing category
NDA · NDA209379
Marketed since
March 28, 2022
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Selenious Acid →

Package NDC codes (1)

Package NDCDescriptionSince
0517-6502-1010 VIAL, SINGLE-DOSE in 1 BOX (0517-6502-10) / 2 mL in 1 VIAL, SINGLE-DOSE (0517-6502-01)Mar 28, 2022

Recalls mentioning this NDC

Other Selenious Acid products