Vimpat
- Product NDC
- 70518-0257
- 11-digit product format
- 705180257
- Labeler code
- 70518
- Product ID
- 70518-0257_a3de63ee-3c38-1347-e053-2a95a90afe7d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lacosamide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- NDA022253
- Marketing category
- NDA
- Marketing start
- 2017-02-23
- Marketing end
- 0000-00-00
- Substance
- LACOSAMIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]
- DEA schedule
- CV
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 70518-0257-0 | 70518025700 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0257-0) | 2017-02-23 | 0000-00-00 | No | No | Current |