NDC 0378-5615 – Levetiracetam

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

Human Prescription Drug 1 recall

Product NDC0378-5615

Product details

Brand name
Levetiracetam
Generic name
Levetiracetam
Labeler
Mylan Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076919
Marketed since
November 4, 2008
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Levetiracetam →

Package NDC codes (2)

Package NDCDescriptionSince
0378-5615-05500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-5615-05)Nov 4, 2008
0378-5615-78120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-5615-78)Nov 4, 2008

Recalls mentioning this NDC

Other Levetiracetam products