Glipizide

Product NDC
50090-7735
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Glipizide
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA214874
Marketing category
ANDA
Substance
GLIPIZIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-7735-090 TABLET in 1 BOTTLE (50090-7735-0) 2025-10-28NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Glipizide Tablets, USP For Oral UseA-S Medication Solutions2025-11-01HUMAN PRESCRIPTION DRUG LABEL1