Levetiracetam
- Product NDC
- 16729-064
- 11-digit product format
- 167290064
- Labeler code
- 16729
- Product ID
- 16729-064_aef10601-69ca-9fd8-e053-2995a90a18e3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- levetiracetam
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Accord Healthcare Inc.
- 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 |
|---|
| 16729-064-16 | 16729006416 | 500 TABLET, FILM COATED in 1 BOTTLE (16729-064-16) | 2013-05-23 | 0000-00-00 | No | No | Current |
| 16729-064-29 | 16729006429 | 120 TABLET, FILM COATED in 1 BOTTLE (16729-064-29) | 2013-05-23 | 0000-00-00 | No | No | Current |