NDC 68001-402 – Levetiracetam

Levetiracetam 250 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC68001-402

Product details

Brand name
Levetiracetam
Generic name
Levetiracetam
Labeler
BluePoint Laboratories
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078993
Marketed since
June 19, 2019
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Levetiracetam →

Package NDC codes (2)

Package NDCDescriptionSince
68001-402-03500 TABLET, FILM COATED in 1 BOTTLE (68001-402-03)Jun 19, 2019
68001-402-07120 TABLET, FILM COATED in 1 BOTTLE (68001-402-07)Jun 19, 2019

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