NDC 67457-187 – Aloprim

Allopurinol Sodium 500 mg/25mL · Injection, Powder, Lyophilized, For Solution · Intravenous

Human Prescription Drug 1 recall

Product NDC67457-187

Product details

Brand name
Aloprim
Generic name
Allopurinol
Labeler
Mylan Institutional LLC
Dosage form
Injection, Powder, Lyophilized, For Solution
Route
Intravenous
Marketing category
NDA · NDA020298
Marketed since
May 15, 2007
Listing expires
December 31, 2026
Pharmacologic class
Xanthine Oxidase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Aloprim →

Package NDC codes (1)

Package NDCDescriptionSince
67457-187-501 VIAL, GLASS in 1 CARTON (67457-187-50) / 25 mL in 1 VIAL, GLASSMay 15, 2007

Recalls mentioning this NDC