ALLOPURINOL

Product NDC
50090-7696
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
ALLOPURINOL
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA217748
Marketing category
ANDA
Substance
ALLOPURINOL
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-7696-330 TABLET in 1 BOTTLE (50090-7696-3) 2025-10-10NoHistorical
50090-7696-490 TABLET in 1 BOTTLE (50090-7696-4) 2025-10-10NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
ALLOPURINOLA-S Medication Solutions2025-10-14Human Prescription Drug Label1