LEVETIRACETAM
- Product NDC
- 51991-651
- 11-digit product format
- 519910651
- Labeler code
- 51991
- Product ID
- 51991-651_9e6c00bc-2eaf-4cd8-be6b-3a5506acfa6b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LEVETIRACETAM
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Breckenridge Pharmaceutical, Inc.
- Application
- ANDA079120
- Marketing category
- ANDA
- Marketing start
- 2013-11-19
- Marketing end
- 2024-12-31
- Substance
- LEVETIRACETAM
- Active strength
- 100 mg/mL
- Pharmacologic classes
- Decreased Central Nervous System Disorganized Electrical Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51991-651-16 | 51991065116 | 473 mL in 1 BOTTLE (51991-651-16) | 473 ml | 2013-11-19 | 0000-00-00 | No | No | Current |