NDC 46708-171 – Lacosamide

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

Human Prescription Drug DEA schedule CV

Product NDC46708-171

Product details

Brand name
Lacosamide
Generic name
Lacosamide
Labeler
Alembic Pharmaceuticals Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA204974
Marketed since
March 18, 2022
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Lacosamide →

Package NDC codes (4)

Package NDCDescriptionSince
46708-171-10100 TABLET, FILM COATED in 1 CARTON (46708-171-10)Mar 18, 2022
46708-171-3030 TABLET, FILM COATED in 1 BOTTLE (46708-171-30)Mar 18, 2022
46708-171-6060 TABLET, FILM COATED in 1 BOTTLE (46708-171-60)Mar 18, 2022
46708-171-911000 TABLET, FILM COATED in 1 BOTTLE (46708-171-91)Mar 18, 2022

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