Levetiracetam
- Product NDC
- 69076-500
- 11-digit product format
- 690760500
- Labeler code
- 69076
- Product ID
- 69076-500_d14f7285-c76a-0bdb-e053-2995a90a5114
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levetiracetam
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Florida Pharmaceutical Products, LLC.
- Application
- ANDA202167
- Marketing category
- ANDA
- Marketing start
- 2016-06-01
- 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 |
|---|
| 69076-500-60 | 69076050060 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69076-500-60) | 2016-06-01 | 0000-00-00 | No | No | Current |