NDC 51991-348 – Lacosamide

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

Human Prescription Drug DEA schedule CV

Product NDC51991-348

Product details

Brand name
Lacosamide
Generic name
Lacosamide
Labeler
Breckenridge Pharmaceutical, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA204921
Marketed since
March 18, 2022
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Lacosamide →

Package NDC codes (2)

Package NDCDescriptionSince
51991-348-05500 TABLET, FILM COATED in 1 BOTTLE (51991-348-05)Mar 18, 2022
51991-348-0660 TABLET, FILM COATED in 1 BOTTLE (51991-348-06)Mar 18, 2022

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