NDC 69539-026 – lacosamide

Lacosamide 100 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug DEA schedule CV

Product NDC69539-026

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
69539-026-05500 TABLET, FILM COATED in 1 BOTTLE (69539-026-05)Mar 19, 2022
69539-026-6060 TABLET, FILM COATED in 1 BOTTLE (69539-026-60)Mar 19, 2022

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