NDC 82804-992 – Lacosamide

Lacosamide 150 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug DEA schedule CV

Product NDC82804-992

Product details

Brand name
Lacosamide
Generic name
Lacosamide
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA205237
Marketed since
July 10, 2023
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Lacosamide →

Package NDC codes (9)

Package NDCDescriptionSince
82804-992-00100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82804-992-00)May 21, 2024
82804-992-111000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82804-992-11)May 21, 2024
82804-992-3030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82804-992-30)May 21, 2024
82804-992-55500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82804-992-55)May 21, 2024
82804-992-6060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82804-992-60)May 21, 2024
82804-992-64240 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82804-992-64)May 21, 2024
82804-992-72120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82804-992-72)May 21, 2024
82804-992-78180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82804-992-78)May 21, 2024
82804-992-9090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82804-992-90)May 21, 2024

Other Lacosamide products