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Levetiracetam

NDC 55111-183 · Dr. Reddy's Laboratories Limited

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

Packages

55111-183-01 — 100 TABLET in 1 BOTTLE (55111-183-01)

55111-183-04 — 120 TABLET in 1 BOTTLE (55111-183-04)

55111-183-05 — 500 TABLET in 1 BOTTLE (55111-183-05)

55111-183-30 — 30 TABLET in 1 BOTTLE (55111-183-30)

55111-183-79 — 1 BLISTER PACK in 1 CARTON (55111-183-79) / 10 TABLET in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50474-597 — levetiracetam, 50474-598 — levetiracetam, 50474-599 — levetiracetam, 51079-821 — levetiracetam, 51224-013 — levetiracetam, 51655-325 — Levetiracetam, 51672-4136 — Levetiracetam, 53041-660 — Levetiracetam, 55111-181 — Levetiracetam, 55111-182 — Levetiracetam, 55111-248 — Levetiracetam, 55150-177 — Levetiracetam, 55150-246 — Levetiracetam in sodium chloride, 55150-247 — Levetiracetam in sodium chloride, 55150-248 — Levetiracetam in sodium chloride, 55154-3367 — Levetiracetam, 55154-4171 — Levetiracetam, 55154-4316 — LEVETIRACETAM, 55154-5699 — levetiracetam, 55154-5782 — 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.