NDC 50474-597 – Keppra

Levetiracetam 1000 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 1 recall

Product NDC50474-597

Product details

Brand name
Keppra
Generic name
Levetiracetam
Labeler
UCB, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA · NDA021035
Marketed since
April 24, 2000
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Keppra →

Package NDC codes (1)

Package NDCDescriptionSince
50474-597-6660 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50474-597-66)Apr 24, 2000

Recalls mentioning this NDC

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