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
- 63629-4137_505a2d97-ea8d-4e3a-9af7-95df7f59d89b
- Product NDC
- 63629-4137
- Form
- TABLET, FILM COATED
- Composition / generic term
- Levetiracetam
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20090115
- Source listing expiry
- 20271231
Source-listed ingredients
- LEVETIRACETAM — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 90 TABLET, FILM COATED in 1 BOTTLE (63629-4137-1) · 63629-4137-1
- 60 TABLET, FILM COATED in 1 BOTTLE (63629-4137-2) · 63629-4137-2
- 30 TABLET, FILM COATED in 1 BOTTLE (63629-4137-3) · 63629-4137-3
- 120 TABLET, FILM COATED in 1 BOTTLE (63629-4137-4) · 63629-4137-4
- 28 TABLET, FILM COATED in 1 BOTTLE (63629-4137-5) · 63629-4137-5
- 100 TABLET, FILM COATED in 1 BOTTLE (63629-4137-6) · 63629-4137-6
- 21 TABLET, FILM COATED in 1 BOTTLE (63629-4137-7) · 63629-4137-7
- 180 TABLET, FILM COATED in 1 BOTTLE (63629-4137-8) · 63629-4137-8
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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