Levetiracetam
- Product NDC
- 71335-0048
- 11-digit product format
- 713350048
- Labeler code
- 71335
- Product ID
- 71335-0048_e72786f4-0fb9-42a5-a655-9702dfbb4cfe
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- levetiracetam
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA090843
- Marketing category
- ANDA
- Marketing start
- 2013-05-31
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0048-1 | 71335004801 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0048-1) | 2014-06-24 | 0000-00-00 | No | No | Current |
| 71335-0048-2 | 71335004802 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0048-2) | 2014-06-24 | 0000-00-00 | No | No | Current |
| 71335-0048-3 | 71335004803 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0048-3) | 2014-06-24 | 0000-00-00 | No | No | Current |
| 71335-0048-4 | 71335004804 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-0048-4) | 2014-06-24 | 0000-00-00 | No | No | Current |
| 71335-0048-5 | 71335004805 | 28 TABLET, FILM COATED in 1 BOTTLE (71335-0048-5) | 2014-06-24 | 0000-00-00 | No | No | Current |