Levetiracetam
- Product NDC
- 71335-0702
- 11-digit product format
- 713350702
- Labeler code
- 71335
- Product ID
- 71335-0702_0f1f4da7-f189-4638-a1ad-056e19185f61
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levetiracetam
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA090515
- Marketing category
- ANDA
- Marketing start
- 2010-10-08
- Substance
- LEVETIRACETAM
- Active strength
- 250 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 |
|---|
| 71335-0702-1 | 71335070201 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0702-1) | 2024-05-30 | No | No | Historical |
| 71335-0702-2 | 71335070202 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0702-2) | 2024-05-30 | No | No | Historical |
| 71335-0702-3 | 71335070203 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-0702-3) | 2024-05-30 | No | No | Historical |
| 71335-0702-4 | 71335070204 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0702-4) | 2024-05-30 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Levetiracetam | Bryant Ranch Prepack | 2024-05-29 | HUMAN PRESCRIPTION DRUG LABEL | 6 |