NDC 69539-027 – Lacosamide

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

Human Prescription Drug DEA schedule CV

Product NDC69539-027

Product details

Brand name
Lacosamide
Generic name
Lacosamide
Labeler
MSN LABORATORIES PRIVATE LIMITED
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA204921
Marketed since
March 19, 2022
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Lacosamide →

Package NDC codes (2)

Package NDCDescriptionSince
69539-027-05500 TABLET, FILM COATED in 1 BOTTLE (69539-027-05)Mar 19, 2022
69539-027-6060 TABLET, FILM COATED in 1 BOTTLE (69539-027-60)Mar 19, 2022

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