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
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code55700-879
Application NumberANDA071586
Product Classification
M
Marketing Category
C73584
G
Generic Name
Allopurinol
Product Specifications
Route of AdministrationORAL
Effective DateAugust 26, 2020
FDA Product Classification
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