Allopurinol
PRODUCT INFORMATION Allopurinol Tablets USP 100 mg and 300 mg Tablets
Approved
Approval ID
5fe03530-5659-4359-bdf9-d752c2f5272f
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Feb 6, 2023
Manufacturers
FDA
A-S Medication Solutions
DUNS: 830016429
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 Code50090-5194
Application NumberANDA203154
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateNovember 18, 2021
Generic NameALLOPURINOL
INGREDIENTS (6)
ALLOPURINOLActive
Quantity: 300 mg in 1 1
Code: 63CZ7GJN5I
Classification: ACTIB
LACTOSE MONOHYDRATEInactive
Code: EWQ57Q8I5X
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
CROSPOVIDONEInactive
Code: 2S7830E561
Classification: IACT
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
POVIDONE K30Inactive
Code: U725QWY32X
Classification: IACT