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
- 63629-9847_069caa22-ea24-4717-bd64-9cc0ec5f0b21
- Product NDC
- 63629-9847
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- LEVETIRACETAM
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20140501
- Source listing expiry
- 20271231
Source-listed ingredients
- LEVETIRACETAM — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 21 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9847-1) · 63629-9847-1
- 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9847-2) · 63629-9847-2
- 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9847-3) · 63629-9847-3
- 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9847-4) · 63629-9847-4
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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