NDC 63629-4137 – Levetiracetam

Levetiracetam 500 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC63629-4137

Product details

Brand name
Levetiracetam
Generic name
Levetiracetam
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078154
Marketed since
January 15, 2009
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Levetiracetam →

Package NDC codes (8)

Package NDCDescriptionSince
63629-4137-190 TABLET, FILM COATED in 1 BOTTLE (63629-4137-1)Feb 18, 2010
63629-4137-260 TABLET, FILM COATED in 1 BOTTLE (63629-4137-2)Sep 6, 2011
63629-4137-330 TABLET, FILM COATED in 1 BOTTLE (63629-4137-3)Feb 24, 2012
63629-4137-4120 TABLET, FILM COATED in 1 BOTTLE (63629-4137-4)Apr 19, 2013
63629-4137-528 TABLET, FILM COATED in 1 BOTTLE (63629-4137-5)Mar 6, 2023
63629-4137-6100 TABLET, FILM COATED in 1 BOTTLE (63629-4137-6)Mar 6, 2023
63629-4137-721 TABLET, FILM COATED in 1 BOTTLE (63629-4137-7)Apr 2, 2024
63629-4137-8180 TABLET, FILM COATED in 1 BOTTLE (63629-4137-8)Apr 2, 2026

Other Levetiracetam products