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Levetiracetam

NDC 50405-301 · SOHM, Inc.

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

Packages

50405-301-01 — 30 TABLET in 1 BOTTLE (50405-301-01)

50405-301-02 — 120 TABLET in 1 BOTTLE (50405-301-02)

50405-301-03 — 500 TABLET in 1 BOTTLE (50405-301-03)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-7775 — Levetiracetam, 50090-7804 — Levetiracetam, 50090-7820 — Levetiracetam, 50228-189 — levetiracetam, 50228-190 — levetiracetam, 50228-470 — Levetiracetam, 50228-471 — Levetiracetam, 50228-472 — Levetiracetam, 50228-473 — Levetiracetam, 50405-300 — Levetiracetam, 50405-302 — Levetiracetam, 50405-303 — Levetiracetam, 50474-001 — levetiracetam, 50474-002 — levetiracetam, 50474-594 — levetiracetam, 50474-595 — levetiracetam, 50474-596 — levetiracetam, 50474-597 — levetiracetam, 50474-598 — levetiracetam, 50474-599 — 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.