Glipizide

Product NDC
50090-6473
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Glipizide
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA074223
Marketing category
ANDA
Substance
GLIPIZIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-6473-030 TABLET in 1 BOTTLE (50090-6473-0) 2023-05-11NoHistorical
50090-6473-160 TABLET in 1 BOTTLE (50090-6473-1) 2023-05-11NoHistorical
50090-6473-2100 TABLET in 1 BOTTLE (50090-6473-2) 2023-05-11NoHistorical
50090-6473-390 TABLET in 1 BOTTLE (50090-6473-3) 2023-05-11NoHistorical
50090-6473-4180 TABLET in 1 BOTTLE (50090-6473-4) 2023-05-11NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
glipiZIDE Tablets, USP for oral use Rx onlyA-S Medication Solutions2025-04-01HUMAN PRESCRIPTION DRUG LABEL3