Active Ingredient: ALLOPURINOL
Proprietary Name: ALLOPURINOL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 100MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A071450
Product Number: 002
Approval Date: Jan 9, 1987
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES INC
Marketing Status:
Prescription
Patent and Exclusivity Information