Skip to main content

Levetiracetam

NDC 0378-5619 · Mylan Pharmaceuticals Inc.

Generic namelevetiracetam
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)LEVETIRACETAM
Strength1000 mg/1
Pharmacologic classDecreased Central Nervous System Disorganized Electrical Activity [PE]
Marketing categoryANDA

Packages

0378-5619-91 — 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-5619-91)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0143-9281 — Levetiracetam in Sodium Chloride, 0143-9282 — Levetiracetam in Sodium Chloride, 0143-9283 — Levetiracetam in Sodium Chloride, 0143-9574 — Levetiracetam, 0143-9673 — Levetiracetam, 0264-1009 — Levetiracetam, 0264-1509 — Levetiracetam, 0264-5009 — Levetiracetam, 0378-5615 — levetiracetam, 0378-5617 — levetiracetam, 0409-1886 — LEVETIRACETAM, 0409-2011 — LEVETIRACETAM, 0472-0235 — Levetiracetam, 0615-8498 — Levetiracetam, 0615-8499 — Levetiracetam, 0615-8500 — Levetiracetam, 0615-8501 — Levetiracetam, 0904-7123 — Levetiracetam, 0904-7124 — Levetiracetam, 0904-7125 — Levetiracetam, +277 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.