Active Ingredient: ALLOPURINOL SODIUM
Proprietary Name: ALLOPURINOL SODIUM
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 500MG BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A076870
Product Number: 001
Approval Date: Aug 26, 2004
Applicant Holder Full Name: HIKMA PHARMACEUTICALS USA INC
Marketing Status:
Prescription
Patent and Exclusivity Information
