Levetiracetam
- Product NDC
- 50090-7820
- 11-digit product format
- 500907820
- Labeler code
- 50090
- Product ID
- 50090-7820_184de745-659c-4ddd-929a-4edc68912baf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levetiracetam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA091491
- Marketing category
- ANDA
- Marketing start
- 2023-05-01
- 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 | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7820-0 | 50090782000 | 120 TABLET in 1 BOTTLE (50090-7820-0) | 120 tablet | 2025-12-11 | No | No | Historical |
| 50090-7820-1 | 50090782001 | 500 TABLET in 1 BOTTLE (50090-7820-1) | 500 tablet | 2025-12-11 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Levetiracetam | A-S Medication Solutions | 2025-12-30 | HUMAN PRESCRIPTION DRUG LABEL | 1 |