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Levetiracetam

NDC 87063-191 · ASCLEMED USA 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

87063-191-12 — 120 TABLET in 1 BOTTLE (87063-191-12)

87063-191-30 — 30 TABLET in 1 BOTTLE (87063-191-30)

87063-191-60 — 60 TABLET in 1 BOTTLE (87063-191-60)

87063-191-90 — 90 TABLET in 1 BOTTLE (87063-191-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

76494-529 — Levetiracetam, 76494-530 — Levetiracetam, 76494-531 — Levetiracetam, 80425-0565 — Levetiracetam, 80425-0566 — Levetiracetam, 80705-100 — levetiracetam, 80705-101 — levetiracetam, 81033-013 — LEVETIRACETAM, 81665-100 — LEVETIRACETAM, 81665-101 — LEVETIRACETAM, 82009-121 — Levetiracetam, 82009-122 — Levetiracetam, 82009-123 — Levetiracetam, 82009-124 — Levetiracetam, 85957-037 — Levetiracetam, 87063-190 — Levetiracetam, 87063-192 — Levetiracetam, 87063-193 — Levetiracetam, 87234-0035 — Levetiracetam, 87441-046 — 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.