Lacosamide

Product NDC
82804-990
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lacosamide
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA205237
Marketing category
ANDA
Substance
LACOSAMIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
82804-990-00100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82804-990-00) 2024-05-21NoHistorical
82804-990-111000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82804-990-11) 2024-05-21NoHistorical
82804-990-3030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82804-990-30) 2024-05-21NoHistorical
82804-990-55500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82804-990-55) 2024-05-21NoHistorical
82804-990-6060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82804-990-60) 2024-05-21NoHistorical
82804-990-64240 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82804-990-64) 2024-05-21NoHistorical
82804-990-72120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82804-990-72) 2024-05-21NoHistorical
82804-990-78180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82804-990-78) 2024-05-21NoHistorical
82804-990-9090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82804-990-90) 2024-05-21NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
LacosamideProficient Rx LP2024-05-01HUMAN PRESCRIPTION DRUG LABEL1