Levetiracetam

NDC 80425-0565 · Advanced Rx of Tennessee, LLC

Generic nameLevetiracetam

Dosage formTABLET

RouteORAL

Active ingredient(s)LEVETIRACETAM

Strength500 mg/1

Pharmacologic classDecreased Central Nervous System Disorganized Electrical Activity [PE]

Marketing categoryANDA

Packages

80425-0565-1 — 120 TABLET in 1 BOTTLE (80425-0565-1)

80425-0565-2 — 30 TABLET in 1 BOTTLE (80425-0565-2)

80425-0565-3 — 60 TABLET in 1 BOTTLE (80425-0565-3)

80425-0565-4 — 90 TABLET in 1 BOTTLE (80425-0565-4)

FDA lists these products with the same active ingredient.

72865-188 — Levetiracetam, 72865-189 — Levetiracetam, 72865-190 — Levetiracetam, 76282-246 — Levetiracetam, 76282-247 — Levetiracetam, 76282-248 — Levetiracetam, 76494-528 — Levetiracetam, 76494-529 — Levetiracetam, 76494-530 — Levetiracetam, 76494-531 — Levetiracetam, 80425-0566 — Levetiracetam, 80705-100 — levetiracetam, 80705-101 — levetiracetam, 81033-013 — LEVETIRACETAM, 81665-100 — LEVETIRACETAM, 81665-101 — LEVETIRACETAM, 82009-121 — Levetiracetam, 82009-122 — Levetiracetam, 82009-123 — Levetiracetam, 82009-124 — 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.