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Levetiracetam

NDC 70010-523 · Granules Pharmaceuticals Inc.

Generic nameLevetiracetam
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)LEVETIRACETAM
Strength750 mg/1
Pharmacologic classDecreased Central Nervous System Disorganized Electrical Activity [PE]
Marketing categoryANDA

Packages

70010-523-03 — 30 TABLET, FILM COATED in 1 BOTTLE (70010-523-03)

70010-523-10 — 1000 TABLET, FILM COATED in 1 BOTTLE (70010-523-10)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69102-105 — Levetiracetam, 69102-106 — Levetiracetam, 69102-107 — Levetiracetam, 69102-108 — Levetiracetam, 69339-157 — Levetiracetam, 69367-332 — Levetiracetam, 69367-333 — Levetiracetam, 69452-412 — LEVETIRACETAM, 70010-521 — Levetiracetam, 70010-522 — 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, 70518-1901 — Levetiracetam, 70518-3803 — Levetiracetam, 70518-3804 — 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.