Allopurinol
ALLOPURINOL TABLETS USP
Approved
Approval ID
df745f5f-7f05-205d-e053-2995a90a05a4
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 18, 2023
Manufacturers
FDA
Northwind Pharmaceuticals
DUNS: 036986393
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Allopurinol
PRODUCT DETAILS
NDC Product Code51655-968
Application NumberANDA071450
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateDecember 18, 2023
Generic NameAllopurinol
INGREDIENTS (1)
ALLOPURINOLActive
Quantity: 300 mg in 1 1
Code: 63CZ7GJN5I
Classification: ACTIB