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Levetiracetam

NDC 50228-190 · ScieGen Pharmaceuticals, Inc

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

Packages

50228-190-05 — 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50228-190-05)

50228-190-30 — 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50228-190-30)

50228-190-60 — 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50228-190-60)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-7521 — Levetiracetam, 50090-7717 — Levetiracetam, 50090-7768 — Levetiracetam, 50090-7770 — Levetiracetam, 50090-7771 — Levetiracetam, 50090-7774 — Levetiracetam, 50090-7775 — Levetiracetam, 50090-7804 — Levetiracetam, 50090-7820 — Levetiracetam, 50228-189 — levetiracetam, 50228-470 — Levetiracetam, 50228-471 — Levetiracetam, 50228-472 — Levetiracetam, 50228-473 — Levetiracetam, 50405-300 — Levetiracetam, 50405-301 — Levetiracetam, 50405-302 — Levetiracetam, 50405-303 — Levetiracetam, 50474-001 — levetiracetam, 50474-002 — 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.