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Levetiracetam

NDC 50090-6086 · A-S Medication Solutions

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

50090-6086-1 — 60 TABLET, FILM COATED in 1 BOTTLE (50090-6086-1)

50090-6086-2 — 180 TABLET, FILM COATED in 1 BOTTLE (50090-6086-2)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

43598-637 — Levetiracetam Injection, 43598-755 — Levetiracetam Injection, 43598-757 — Levetiracetam Injection, 43598-759 — Levetiracetam Injection, 44567-501 — Levetiracetam, 44567-502 — Levetiracetam, 44567-503 — Levetiracetam, 48433-052 — levetiracetam, 50090-1333 — Levetiracetam, 50090-2875 — Levetiracetam, 50090-6378 — Levetiracetam, 50090-7333 — Levetiracetam, 50090-7521 — Levetiracetam, 50090-7717 — Levetiracetam, 50090-7768 — Levetiracetam, 50090-7770 — Levetiracetam, 50090-7771 — Levetiracetam, 50090-7774 — Levetiracetam, 50090-7775 — Levetiracetam, 50090-7804 — 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.