Levetiracetam
- Product NDC
- 68788-7534
- 11-digit product format
- 687887534
- Labeler code
- 68788
- Product ID
- 68788-7534_67aa79e0-5a80-4cea-b315-f0fa11b68489
- 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
- 2012-09-11
- 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
- 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 |
|---|
| 68788-7534-1 | 68788753401 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-7534-1) | 2019-10-04 | 0000-00-00 | No | No | Current |
| 68788-7534-2 | 68788753402 | 20 TABLET, FILM COATED in 1 BOTTLE (68788-7534-2) | 2019-10-04 | 0000-00-00 | No | No | Current |
| 68788-7534-3 | 68788753403 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-7534-3) | 2019-10-04 | 0000-00-00 | No | No | Current |
| 68788-7534-6 | 68788753406 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-7534-6) | 2019-10-04 | 0000-00-00 | No | No | Current |
| 68788-7534-9 | 68788753409 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-7534-9) | 2019-10-04 | 0000-00-00 | No | No | Current |