Lacosamide
- Product NDC
- 47335-918
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lacosamide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Application
- ANDA205031
- Marketing category
- ANDA
- Substance
- LACOSAMIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 47335-918-18 | 1000 TABLET, FILM COATED in 1 BOTTLE (47335-918-18) | 2022-03-19 | | No | Historical |
| 47335-918-82 | 180 TABLET, FILM COATED in 1 BOTTLE (47335-918-82) | 2022-03-19 | | No | Historical |
| 47335-918-86 | 60 TABLET, FILM COATED in 1 BOTTLE (47335-918-86) | 2022-03-19 | | No | Historical |