NDC 82804-990 – Lacosamide

Lacosamide 50 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug DEA schedule CV

Product NDC82804-990

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

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