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Levetiracetam

NDC 71335-9757 · Bryant Ranch Prepack

Generic nameLevetiracetam
Dosage formTABLET
RouteORAL
Active ingredient(s)LEVETIRACETAM
Strength500 mg/1
Pharmacologic classDecreased Central Nervous System Disorganized Electrical Activity [PE]
Marketing categoryANDA

Packages

71335-9757-1 90 TABLET in 1 BOTTLE (71335-9757-1)

71335-9757-2 60 TABLET in 1 BOTTLE (71335-9757-2)

71335-9757-3 30 TABLET in 1 BOTTLE (71335-9757-3)

71335-9757-4 120 TABLET in 1 BOTTLE (71335-9757-4)

71335-9757-5 28 TABLET in 1 BOTTLE (71335-9757-5)

71335-9757-6 100 TABLET in 1 BOTTLE (71335-9757-6)

71335-9757-7 21 TABLET in 1 BOTTLE (71335-9757-7)

71335-9757-8 180 TABLET in 1 BOTTLE (71335-9757-8)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70518-4306 — Levetiracetam, 70752-203 — LEVETIRACETAM, 71205-728 — Levetiracetam, 71205-880 — Levetiracetam, 71205-881 — Levetiracetam, 71335-0694 — Levetiracetam, 71335-0702 — Levetiracetam, 71335-2098 — Levetiracetam, 71335-2275 — Levetiracetam, 71335-2282 — Levetiracetam, 72162-2638 — Levetiracetam, 72162-2639 — levetiracetam, 72162-2667 — LEVETIRACETAM, 72189-190 — LEVETIRACETAM, 72189-229 — LEVETIRACETAM, 72189-510 — Levetiracetam ER, 72189-679 — Levetiracetam, 72205-037 — levetiracetam, 72205-094 — Levetiracetam, 72205-095 — 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.