Allopurinol
Allopurinol Tablets
Approved
Approval ID
dc2174d5-4d32-4731-9f0d-b649981c5198
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Aug 26, 2020
Manufacturers
FDA
Quality Care Products, LLC
DUNS: 831276758
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 Code55700-879
Application NumberANDA071586
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateAugust 26, 2020
Generic NameAllopurinol
INGREDIENTS (5)
AllopurinolActive
Quantity: 100 mg in 1 1
Code: 63CZ7GJN5I
Classification: ACTIB
Magnesium stearateInactive
Code: 70097M6I30
Classification: IACT
Lactose, Unspecified FormInactive
Code: J2B2A4N98G
Classification: IACT
povidoneInactive
Code: FZ989GH94E
Classification: IACT
STARCH, POTATOInactive
Code: 8I089SAH3T
Classification: IACT