Levetiracetam

Product NDC
65162-528
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Levetiracetam
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Amneal Pharmaceuticals LLC
Application
ANDA090767
Marketing category
ANDA
Substance
LEVETIRACETAM
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
65162-528-16120 TABLET, FILM COATED in 1 BOTTLE (65162-528-16) 2013-02-28NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
LevetiracetamAmneal Pharmaceuticals LLC2017-11-28HUMAN PRESCRIPTION DRUG LABEL26