Levetiracetam
- Product NDC
- 50090-7768
- 11-digit product format
- 500907768
- Labeler code
- 50090
- Product ID
- 50090-7768_7ae37a19-2a35-4bfd-92f2-4a982a5d1023
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levetiracetam
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA078993
- Marketing category
- ANDA
- Marketing start
- 2009-01-15
- Substance
- LEVETIRACETAM
- Active strength
- 500 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 | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7768-0 | 50090776800 | 120 TABLET, FILM COATED in 1 BOTTLE (50090-7768-0) | 2025-11-17 | No | No | Historical |
| 50090-7768-1 | 50090776801 | 500 TABLET, FILM COATED in 1 BOTTLE (50090-7768-1) | 2025-11-17 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Levetiracetam | A-S Medication Solutions | 2025-11-19 | Human Prescription Drug Label | 1 |