Levetiracetam
- Product NDC
- 50090-2815
- 11-digit product format
- 500902815
- Labeler code
- 50090
- Product ID
- 50090-2815_b38367f8-3705-4a8a-b380-2802f7a763cb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levetiracetam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA078858
- Marketing category
- ANDA
- Marketing start
- 2009-01-15
- Marketing end
- 0000-00-00
- Substance
- LEVETIRACETAM
- Active strength
- 500 mg/1
- Pharmacologic classes
- Decreased Central Nervous System Disorganized Electrical Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 44YRR34555 | LEVETIRACETAM | 102767-28-2 | LEVETIRACETAM |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Levetiracetam | A-S Medication Solutions | 2018-08-29 | HUMAN PRESCRIPTION DRUG LABEL | 6 |