Levetiracetam

NDC 76494-528 · Prinston Pharmaceutical Inc.

Generic nameLevetiracetam

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)LEVETIRACETAM

Strength250 mg/1

Pharmacologic classDecreased Central Nervous System Disorganized Electrical Activity [PE]

Marketing categoryANDA

Packages

76494-528-12 — 120 TABLET, FILM COATED in 1 BOTTLE (76494-528-12)

FDA lists these products with the same active ingredient.

72485-106 — LEVETIRACETAM, 72572-360 — Levetiracetam, 72789-152 — Levetiracetam, 72865-187 — Levetiracetam, 72865-188 — Levetiracetam, 72865-189 — Levetiracetam, 72865-190 — Levetiracetam, 76282-246 — Levetiracetam, 76282-247 — Levetiracetam, 76282-248 — Levetiracetam, 76494-529 — Levetiracetam, 76494-530 — Levetiracetam, 76494-531 — Levetiracetam, 80425-0565 — Levetiracetam, 80425-0566 — Levetiracetam, 80705-100 — levetiracetam, 80705-101 — levetiracetam, 81033-013 — LEVETIRACETAM, 81665-100 — LEVETIRACETAM, 81665-101 — LEVETIRACETAM, +277 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.