Allopurinol sodium

FDA Drug Profile — Allopurinol sodium

Allopurinol sodium is listed in the FDA National Drug Code directory with 1 NDC code, marketed under brand name including Allopurinol sodium. Available dosage form: injection, powder, lyophilized, for solution.

Drug Details

Generic Name
Allopurinol sodium
Brand Names
Allopurinol sodium
Application Number
ANDA076870
Sponsor
Hikma Pharmaceuticals USA Inc.
NDC Codes
1
Dosage Forms
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients
ALLOPURINOL SODIUM

Indications and Usage

1 INDICATIONS AND USAGE Allopurinol Sodium for Injection is indicated for the management of adult and pediatric patients with leukemia, lymphoma, and solid tumor malignancies who are receiving cancer therapy which causes elevations of serum and urinary uric acid levels and who cannot tolerate oral therapy. Allopurinol Sodium for Injection is a xanthine oxidase inhibitor indicated for the management of adult and pediatric patients with leukemia, lymphoma, and solid tumor malignancies who are receiving cancer therapy which causes elevations of serum and urinary uric acid levels and who cannot tolerate oral therapy. ( 1 )