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Levetiracetam

NDC 67046-1615 · Coupler LLC

Generic nameLevetiracetam
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)LEVETIRACETAM
Strength750 mg/1
Pharmacologic classDecreased Central Nervous System Disorganized Electrical Activity [PE]
Marketing categoryANDA

Packages

67046-1615-3 — 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1615-3)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

66298-0427 — LEVETIRACETAM, 66298-0447 — LEVETIRACETAM, 66298-0467 — LEVETIRACETAM, 66993-100 — levetiracetam, 66993-101 — levetiracetam, 67046-0420 — Levetiracetam, 67046-0863 — Levetiracetam, 67046-0880 — Levetiracetam, 67046-1207 — Levetiracetam, 67046-1461 — Levetiracetam, 67046-2094 — Levetiracetam, 67457-255 — Levetiracetam, 67457-265 — Levetiracetam, 67457-266 — Levetiracetam, 67457-790 — levetiracetam, 67877-768 — Levetiracetam, 67877-769 — Levetiracetam, 67877-770 — Levetiracetam, 67877-771 — Levetiracetam, 68001-113 — 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