Vimpat
- Product NDC
- 0131-2470
- 11-digit product format
- 001312470
- Labeler code
- 0131
- Product ID
- 0131-2470_9462a3cb-199d-430a-ade1-87626aa2ffb9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lacosamide
- Dosage form
- KIT
- Labeler
- UCB, Inc.
- Application
- NDA022253
- Marketing category
- NDA
- Marketing start
- 2009-05-26
- Marketing end
- 0000-00-00
- Active strength
- 0
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0131-2470-99 | 00131247099 | 1 BLISTER PACK in 1 CARTON (0131-2470-99) > 1 KIT in 1 BLISTER PACK | 1 blister pack | 2009-05-26 | 0000-00-00 | No | No | Current |