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Levetiracetam

NDC 76494-529 · Prinston Pharmaceutical Inc.

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

76494-529-12 — 120 TABLET, FILM COATED in 1 BOTTLE (76494-529-12)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72572-360 — Levetiracetam, 72789-152 — Levetiracetam, 72865-187 — Levetiracetam, 72865-188 — Levetiracetam, 72865-189 — Levetiracetam, 72865-190 — Levetiracetam, 76282-246 — Levetiracetam, 76282-247 — Levetiracetam, 76282-248 — Levetiracetam, 76494-528 — 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, +277 more

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

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels