Levetiracetam
- Product NDC
- 68788-7074
- 11-digit product format
- 687887074
- Labeler code
- 68788
- Product ID
- 68788-7074_d694befc-990d-4ddc-ba85-370acfa4d9a9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levetiracetam
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA078106
- Marketing category
- ANDA
- Marketing start
- 2018-01-02
- 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
- 2022-12-31
- 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 |
|---|
| 68788-7074-1 | 68788707401 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-7074-1) | 2018-01-02 | 0000-00-00 | No | No | Current |
| 68788-7074-2 | 68788707402 | 20 TABLET, FILM COATED in 1 BOTTLE (68788-7074-2) | 2018-01-02 | 0000-00-00 | No | No | Current |
| 68788-7074-3 | 68788707403 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-7074-3) | 2018-01-02 | 0000-00-00 | No | No | Current |
| 68788-7074-6 | 68788707406 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-7074-6) | 2018-01-02 | 0000-00-00 | No | No | Current |
| 68788-7074-9 | 68788707409 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-7074-9) | 2018-01-02 | 0000-00-00 | No | No | Current |