NDC 69367-348 – Lacosamide

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

Human Prescription Drug DEA schedule CV

Product NDC69367-348

Product details

Brand name
Lacosamide
Generic name
Lacosamide
Labeler
Westminster Pharmaceuticals, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA205237
Marketed since
July 10, 2023
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Lacosamide →

Package NDC codes (1)

Package NDCDescriptionSince
69367-348-6060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69367-348-60)Jul 10, 2023

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