NDC 65862-747 – Lacosamide

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

Human Prescription Drug DEA schedule CV

Product NDC65862-747

Product details

Brand name
Lacosamide
Generic name
Lacosamide
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA204994
Marketed since
January 5, 2023
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Lacosamide →

Package NDC codes (2)

Package NDCDescriptionSince
65862-747-033 BLISTER PACK in 1 CARTON (65862-747-03) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-747-10)Jan 5, 2023
65862-747-6060 TABLET, FILM COATED in 1 BOTTLE (65862-747-60)Jan 5, 2023

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