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
- 72189-190_4c4bd407-ac66-f594-e063-6294a90a31fe
- Product NDC
- 72189-190
- Form
- TABLET, FILM COATED
- Composition / generic term
- LEVETIRACETAM
- Labeler
- DIRECT RX
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210607
- Source listing expiry
- 20271231
Source-listed ingredients
- LEVETIRACETAM — 250 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE (72189-190-30) · 72189-190-30
- 60 TABLET, FILM COATED in 1 BOTTLE (72189-190-60) · 72189-190-60
- 120 TABLET, FILM COATED in 1 BOTTLE (72189-190-72) · 72189-190-72
- 90 TABLET, FILM COATED in 1 BOTTLE (72189-190-90) · 72189-190-90
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →