Levetiracetam

Product NDC
50090-7804
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Levetiracetam
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA215069
Marketing category
ANDA
Substance
LEVETIRACETAM
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-7804-160 TABLET, FILM COATED in 1 BOTTLE (50090-7804-1) 2025-12-01NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
LevetiracetamA-S Medication Solutions2025-12-30HUMAN PRESCRIPTION DRUG LABEL1