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
- 0121-4799_f63f4202-d0c1-4ef3-8dc5-8bb4cab6a613
- Product NDC
- 0121-4799
- Form
- SOLUTION
- Composition / generic term
- LEVETIRACETAM
- Labeler
- PAI Holdings, LLC dba PAI Pharma
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20150604
- Source listing expiry
- 20261231
Source-listed ingredients
- LEVETIRACETAM — 500 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 4 TRAY in 1 CASE (0121-4799-40) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (0121-4799-05) · 0121-4799-40
- 5 TRAY in 1 CASE (0121-4799-50) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (0121-4799-05) · 0121-4799-50
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 →