Levetiracetam

Product NDC
71205-880
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Levetiracetam
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA205130
Marketing category
ANDA
Substance
LEVETIRACETAM
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
71205-880-00100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71205-880-00) 2021-11-05NoHistorical
71205-880-111000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71205-880-11) 2021-11-05NoHistorical
71205-880-3030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71205-880-30) 2021-11-05NoHistorical
71205-880-55500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71205-880-55) 2021-11-05NoHistorical
71205-880-6060 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71205-880-60) 2021-11-05NoHistorical
71205-880-64240 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71205-880-64) 2021-11-05NoHistorical
71205-880-72120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71205-880-72) 2021-11-05NoHistorical
71205-880-78180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71205-880-78) 2021-11-05NoHistorical
71205-880-9090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71205-880-90) 2021-11-05NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Levetiracetam ERProficient Rx LP2022-04-01HUMAN PRESCRIPTION DRUG LABEL2