United States · FDA National Drug Code directory

Levetiracetam

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
68180-118_8690e365-04d0-44ee-98ec-281e438ee0b0
Product NDC
68180-118
Form
TABLET, EXTENDED RELEASE
Composition / generic term
Levetiracetam
Labeler
Lupin Pharmaceuticals, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20110912
Source listing expiry
20261231

Source-listed ingredients

  • LEVETIRACETAM — 750 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-118-07) · 68180-118-07

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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