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Levetiracetam

NDC 70518-4125 · REMEDYREPACK INC.

Generic nameLevetiracetam
Dosage formTABLET, FILM COATED, EXTENDED RELEASE
RouteORAL
Active ingredient(s)LEVETIRACETAM
Strength500 mg/1
Pharmacologic classDecreased Central Nervous System Disorganized Electrical Activity [PE]
Marketing categoryANDA

Packages

70518-4125-0 — 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-4125-0)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70069-847 — Levetiracetam in Sodium Chloride, 70518-1108 — Levetiracetam, 70518-1772 — Levetiracetam, 70518-1796 — Levetiracetam, 70518-1901 — Levetiracetam, 70518-3803 — Levetiracetam, 70518-3804 — Levetiracetam, 70518-3895 — Levetiracetam, 70518-4005 — LEVETIRACETAM, 70518-4013 — Levetiracetam, 70518-4301 — Levetiracetam, 70518-4306 — Levetiracetam, 70752-203 — LEVETIRACETAM, 71205-728 — Levetiracetam, 71205-880 — Levetiracetam, 71205-881 — Levetiracetam, 71335-0694 — Levetiracetam, 71335-0702 — Levetiracetam, 71335-2098 — Levetiracetam, 71335-2275 — 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.