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
- 60505-3280_24652d3c-86ad-7b6e-6a54-d0a6f952c913
- Product NDC
- 60505-3280
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- Levetiracetam
- Labeler
- Apotex Corp.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20110912
- Source listing expiry
- 20271231
Source-listed ingredients
- LEVETIRACETAM — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60505-3280-5) · 60505-3280-5
- 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60505-3280-6) · 60505-3280-6
- 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60505-3280-8) · 60505-3280-8
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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