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
- 71335-9757_78a08eac-4bd1-4c6e-ba0a-4a71f5d4b7af
- Product NDC
- 71335-9757
- Form
- TABLET
- Composition / generic term
- Levetiracetam
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230501
- Source listing expiry
- 20271231
Source-listed ingredients
- LEVETIRACETAM — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 90 TABLET in 1 BOTTLE (71335-9757-1) · 71335-9757-1
- 60 TABLET in 1 BOTTLE (71335-9757-2) · 71335-9757-2
- 30 TABLET in 1 BOTTLE (71335-9757-3) · 71335-9757-3
- 120 TABLET in 1 BOTTLE (71335-9757-4) · 71335-9757-4
- 28 TABLET in 1 BOTTLE (71335-9757-5) · 71335-9757-5
- 100 TABLET in 1 BOTTLE (71335-9757-6) · 71335-9757-6
- 21 TABLET in 1 BOTTLE (71335-9757-7) · 71335-9757-7
- 180 TABLET in 1 BOTTLE (71335-9757-8) · 71335-9757-8
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 →