Levetiracetam
- Product NDC
- 54838-548
- 11-digit product format
- 548380548
- Labeler code
- 54838
- Product ID
- 54838-548_1b579b0a-d818-4dde-8f87-075b58baa58d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levetiracetam
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Lannett Company, Inc.
- Application
- ANDA090263
- Marketing category
- ANDA
- Marketing start
- 2009-04-03
- Marketing end
- 2023-02-28
- 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 |
|---|
| 54838-548-80 | 54838054880 | 473 mL in 1 BOTTLE, PLASTIC (54838-548-80) | 473 ml | 2009-04-03 | 2023-02-28 | No | No | Current |