Lacosamide
- Product NDC
- 66689-110
- 11-digit product format
- 666890110
- Labeler code
- 66689
- Product ID
- 66689-110_8164ec13-4fbf-410d-8238-b73beb3034cd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lacosamide
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- VistaPharm, Inc.
- Application
- NDA022255
- Marketing category
- NDA
- Marketing start
- 2021-11-15
- Marketing end
- 0000-00-00
- Substance
- LACOSAMIDE
- Active strength
- 200 mg/20mL
- Pharmacologic classes
- Decreased Central Nervous System Disorganized Electrical Activity [PE]
- DEA schedule
- CV
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 66689-110-10 | 66689011010 | 10 CUP, UNIT-DOSE in 1 CASE (66689-110-10) > 20 mL in 1 CUP, UNIT-DOSE (66689-110-01) | 2021-11-15 | 0000-00-00 | No | No | Current |