Allopurinol
ALLOPURINOL TABLETS USP 022
Approved
Approval ID
57fa94ed-b29e-456a-e053-2a91aa0af484
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Aug 30, 2017
Manufacturers
FDA
Contract Pharmacy Services-PA
DUNS: 945429777
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 Code67046-022
Application NumberANDA071450
Product Classification
M
Marketing Category
C73584
G
Generic Name
Allopurinol
Product Specifications
Route of AdministrationORAL
Effective DateAugust 30, 2017
FDA Product Classification
INGREDIENTS (1)
ALLOPURINOLActive
Quantity: 100 mg in 1 1
Code: 63CZ7GJN5I
Classification: ACTIB