Allopurinol
ALLOPURINOL TABLETS USP
Approved
Approval ID
b2ab2389-ccaf-487b-9985-50e3539e7617
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Apr 7, 2023
Manufacturers
FDA
PD-Rx Pharmaceuticals, Inc.
DUNS: 156893695
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 Code43063-975
Application NumberANDA071450
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateApril 7, 2023
Generic NameAllopurinol
INGREDIENTS (1)
ALLOPURINOLActive
Quantity: 100 mg in 1 1
Code: 63CZ7GJN5I
Classification: ACTIB