Levetiracetam
- Product NDC
- 71335-0093
- 11-digit product format
- 713350093
- Labeler code
- 71335
- Product ID
- 71335-0093_e30ff055-8381-4a66-b90c-666adccc3630
- 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
- 2013-05-23
- Marketing end
- 0000-00-00
- Substance
- LEVETIRACETAM
- Active strength
- 250 mg/1
- Pharmacologic classes
- Decreased Central Nervous System Disorganized Electrical Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 71335-0093-1 | 71335009301 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0093-1) | 2014-06-06 | 0000-00-00 | No | No | Current |
| 71335-0093-2 | 71335009302 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0093-2) | 2014-06-06 | 0000-00-00 | No | No | Current |
| 71335-0093-3 | 71335009303 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-0093-3) | 2014-06-06 | 0000-00-00 | No | No | Current |
| 71335-0093-4 | 71335009304 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0093-4) | 2014-06-06 | 0000-00-00 | No | No | Current |