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Levetiracetam

NDC 50090-7768 · A-S Medication Solutions

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

Packages

50090-7768-0 — 120 TABLET, FILM COATED in 1 BOTTLE (50090-7768-0)

50090-7768-1 — 500 TABLET, FILM COATED in 1 BOTTLE (50090-7768-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

44567-502 — Levetiracetam, 44567-503 — Levetiracetam, 48433-052 — levetiracetam, 50090-1333 — Levetiracetam, 50090-2875 — Levetiracetam, 50090-6086 — Levetiracetam, 50090-6378 — Levetiracetam, 50090-7333 — Levetiracetam, 50090-7521 — Levetiracetam, 50090-7717 — Levetiracetam, 50090-7770 — Levetiracetam, 50090-7771 — Levetiracetam, 50090-7774 — Levetiracetam, 50090-7775 — Levetiracetam, 50090-7804 — Levetiracetam, 50090-7820 — Levetiracetam, 50228-189 — levetiracetam, 50228-190 — levetiracetam, 50228-470 — Levetiracetam, 50228-471 — 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.