Allopurinol

Product NDC
50090-7353
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
50090-7353-090 TABLET in 1 BOTTLE (50090-7353-0) 2024-10-16NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Allopurinol Tablets, USP 100 mg Scored Tablets and 300 mg Scored Tablets Rx OnlyA-S Medication Solutions2024-10-21HUMAN PRESCRIPTION DRUG LABEL1