Allopurinol

Product NDC
50090-6715
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Allopurinol
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA204467
Marketing category
ANDA
Substance
ALLOPURINOL
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-6715-330 TABLET in 1 BOTTLE (50090-6715-3) 2023-10-05NoHistorical
50090-6715-490 TABLET in 1 BOTTLE (50090-6715-4) 2023-10-05NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
AllopurinolA-S Medication Solutions2024-12-24Human Prescription Drug Label4