Levetiracetam
- Product NDC
- 76282-248
- 11-digit product format
- 762820248
- Labeler code
- 76282
- Product ID
- 76282-248_b044e723-e969-45fa-a4e6-159bfb65267a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levetiracetam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Exelan Pharmaceuticals, Inc.
- Application
- ANDA078234
- Marketing category
- ANDA
- Marketing start
- 2009-01-15
- Substance
- LEVETIRACETAM
- Active strength
- 750 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 |
|---|
| 76282-248-12 | 76282024812 | 120 TABLET in 1 BOTTLE (76282-248-12) | 120 tablet | 2009-01-15 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Levetiracetam | Exelan Pharmaceuticals, Inc. | InvaGen Pharmaceuticals, Inc | 2018-11-29 | HUMAN PRESCRIPTION DRUG LABEL | 4 |