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Levetiracetam

NDC 69367-332 · Westminster Pharmaceuticals, LLC

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

69367-332-60 — 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (69367-332-60)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68180-118 — Levetiracetam, 68788-7884 — Levetiracetam, 68788-8254 — Levetiracetam, 68788-8843 — Levetiracetam, 68999-548 — LEVETIRACETAM, 69102-105 — Levetiracetam, 69102-106 — Levetiracetam, 69102-107 — Levetiracetam, 69102-108 — Levetiracetam, 69339-157 — Levetiracetam, 69367-333 — Levetiracetam, 69452-412 — LEVETIRACETAM, 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, +277 more

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