Glimepiride

Product NDC
50090-6910
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Glimepiride
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA077091
Marketing category
ANDA
Substance
GLIMEPIRIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-6910-090 TABLET in 1 BOTTLE (50090-6910-0) 2023-12-12NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
GlimepirideA-S Medication Solutions2023-12-17HUMAN PRESCRIPTION DRUG LABEL4