NDC 68083-380 – Allopurinol

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

Human Prescription Drug

Product NDC68083-380

Product details

Brand name
Allopurinol
Generic name
Allopurinol
Labeler
Gland Pharma Limited
Dosage form
Injection, Powder, Lyophilized, For Solution
Route
Intravenous
Marketing category
ANDA · ANDA212363
Marketed since
January 26, 2022
Listing expires
December 31, 2026
Pharmacologic class
Xanthine Oxidase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Allopurinol →

Package NDC codes (1)

Package NDCDescriptionSince
68083-380-011 VIAL, GLASS in 1 CARTON (68083-380-01) / 25 mL in 1 VIAL, GLASSJan 26, 2022

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