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
- 70069-846_1baa5928-7efe-4b91-94d6-787335ae60bd
- Product NDC
- 70069-846
- Form
- INJECTION
- Composition / generic term
- Levetiracetam in Sodium Chloride
- Labeler
- Somerset Therapeutics, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260420
- Source listing expiry
- 20271231
Source-listed ingredients
- LEVETIRACETAM — 1000 mg/100mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 POUCH in 1 CASE (70069-846-10) / 1 BAG in 1 POUCH (70069-846-01) / 100 mL in 1 BAG · 70069-846-10
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 →