NDC 0378-5619 – Levetiracetam

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

Human Prescription Drug 1 recall

Product NDC0378-5619

Product details

Brand name
Levetiracetam
Generic name
levetiracetam
Labeler
Mylan Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090261
Marketed since
December 10, 2009
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Levetiracetam →

Package NDC codes (1)

Package NDCDescriptionSince
0378-5619-9160 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-5619-91)Dec 10, 2009

Recalls mentioning this NDC

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