Levetiracetam
- Product NDC
- 50090-7717
- 11-digit product format
- 500907717
- Labeler code
- 50090
- Product ID
- 50090-7717_453bcdb0-0e8d-46eb-b377-d889c3333d85
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levetiracetam
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA090767
- Marketing category
- ANDA
- Marketing start
- 2024-06-10
- 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 |
|---|
| 50090-7717-0 | 50090771700 | 120 TABLET, FILM COATED in 1 BOTTLE (50090-7717-0) | 2025-10-15 | No | No | Historical |
| 50090-7717-1 | 50090771701 | 60 TABLET, FILM COATED in 1 BOTTLE (50090-7717-1) | 2025-10-15 | No | No | Historical |
| 50090-7717-2 | 50090771702 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-7717-2) | 2025-10-15 | No | No | Historical |
| 50090-7717-3 | 50090771703 | 180 TABLET, FILM COATED in 1 BOTTLE (50090-7717-3) | 2025-10-15 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Levetiracetam | A-S Medication Solutions | 2025-10-16 | Human Prescription Drug Label | 1 |