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ELEPSIA XR 1000 MG

NDC 80705-100 · TRIPOINT THERAPEUTICS, LLC

Generic namelevetiracetam
Dosage formTABLET, EXTENDED RELEASE
RouteORAL
Active ingredient(s)LEVETIRACETAM
Strength1000 mg/1
Pharmacologic classDecreased Central Nervous System Disorganized Electrical Activity [PE]
Marketing categoryNDA

Packages

80705-100-02 — 1 BLISTER PACK in 1 CARTON (80705-100-02) / 2 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

80705-100-30 — 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (80705-100-30)

80705-100-99 — 1 BLISTER PACK in 1 CARTON (80705-100-99) / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72865-190 — Levetiracetam, 76282-246 — Levetiracetam, 76282-247 — Levetiracetam, 76282-248 — Levetiracetam, 76494-528 — Levetiracetam, 76494-529 — Levetiracetam, 76494-530 — Levetiracetam, 76494-531 — Levetiracetam, 80425-0565 — Levetiracetam, 80425-0566 — Levetiracetam, 80705-101 — levetiracetam, 81033-013 — LEVETIRACETAM, 81665-100 — LEVETIRACETAM, 81665-101 — LEVETIRACETAM, 82009-121 — Levetiracetam, 82009-122 — Levetiracetam, 82009-123 — Levetiracetam, 82009-124 — Levetiracetam, 85957-037 — Levetiracetam, 87063-190 — Levetiracetam, +277 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.