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Levetiracetam

NDC 70518-1901 · REMEDYREPACK 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

70518-1901-1 — 30 POUCH in 1 BOX (70518-1901-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-1901-2)

70518-1901-3 — 50 POUCH in 1 BOX (70518-1901-3) / 1 TABLET, FILM COATED in 1 POUCH (70518-1901-2)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70010-521 — Levetiracetam, 70010-522 — Levetiracetam, 70010-523 — Levetiracetam, 70010-524 — Levetiracetam, 70069-845 — Levetiracetam in Sodium Chloride, 70069-846 — Levetiracetam in Sodium Chloride, 70069-847 — Levetiracetam in Sodium Chloride, 70518-1108 — Levetiracetam, 70518-1772 — Levetiracetam, 70518-1796 — Levetiracetam, 70518-3803 — Levetiracetam, 70518-3804 — Levetiracetam, 70518-3895 — Levetiracetam, 70518-4005 — LEVETIRACETAM, 70518-4013 — Levetiracetam, 70518-4125 — Levetiracetam, 70518-4301 — Levetiracetam, 70518-4306 — Levetiracetam, 70752-203 — LEVETIRACETAM, 71205-728 — 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.