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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 212363

ALLOPURINOL SODIUM (ALLOPURINOL SODIUM)
EQ 500MG BASE/VIAL
Marketing Status: Prescription
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: A212363
Product Number: 001
Approval Date: Jan 26, 2022
Applicant Holder Full Name: GLAND PHARMA LTD
Marketing Status:  Prescription
Patent and Exclusivity Information
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