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Levetiracetam

NDC 16714-537 · NorthStar RxLLC

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

16714-537-01 — 120 TABLET, FILM COATED in 1 BOTTLE (16714-537-01)

16714-537-02 — 500 TABLET, FILM COATED in 1 BOTTLE (16714-537-02)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

13668-017 — Levetiracetam, 13668-272 — LEVETIRACETAM, 13668-300 — LEVETIRACETAM, 14789-110 — Levetiracetam, 14789-220 — Levetiracetam, 14789-330 — Levetiracetam, 16714-034 — Levetiracetam, 16714-035 — Levetiracetam, 16714-310 — Levetiracetam, 16714-358 — Levetiracetam, 17856-0574 — Levetiracetam, 25021-793 — levetiracetam, 25021-794 — levetiracetam, 25021-795 — levetiracetam, 27808-263 — Levetiracetam, 27808-264 — Levetiracetam, 27808-265 — Levetiracetam, 27808-266 — Levetiracetam, 31722-536 — Levetiracetam, 31722-537 — 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