Lacosamide
- Product NDC
- 70518-4505
- 11-digit product format
- 705184505
- Labeler code
- 70518
- Product ID
- 70518-4505_4120061a-dbb2-8918-e063-6394a90afbf2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lacosamide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA204974
- Marketing category
- ANDA
- Marketing start
- 2025-10-14
- Substance
- LACOSAMIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Decreased Central Nervous System Disorganized Electrical Activity [PE]
- DEA schedule
- CV
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 563KS2PQY5 | LACOSAMIDE | 175481-36-4 | LACOSAMIDE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-4505-0 | 70518450500 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4505-0) | 2025-10-14 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Lacosamide | REMEDYREPACK INC. | 2025-10-14 | HUMAN PRESCRIPTION DRUG LABEL | 1 |