Glipizide

Product NDC
50090-7405
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Glipizide
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA074497
Marketing category
ANDA
Substance
GLIPIZIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-7405-090 TABLET in 1 BOTTLE (50090-7405-0) 2024-10-24NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Glipizide Tablets USPA-S Medication Solutions2024-10-25HUMAN PRESCRIPTION DRUG LABEL1