Levetiracetam
- Product NDC
- 67046-1461
- 11-digit product format
- 670461461
- Labeler code
- 67046
- Product ID
- 67046-1461_2d594515-8a06-02f6-e063-6294a90a7038
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levetiracetam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Coupler LLC
- Application
- ANDA091491
- Marketing category
- ANDA
- Marketing start
- 2025-02-04
- Substance
- LEVETIRACETAM
- Active strength
- 1000 mg/1
- Pharmacologic classes
- Decreased Central Nervous System Disorganized Electrical Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 44YRR34555 | LEVETIRACETAM | 102767-28-2 | LEVETIRACETAM |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 67046-1461-3 | 67046146103 | 30 TABLET in 1 BLISTER PACK (67046-1461-3) | 30 tablet | 2025-02-04 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Levetiracetam | Coupler LLC | 2025-02-04 | HUMAN PRESCRIPTION DRUG LABEL | 1 |