NDC 51991-351 – Lacosamide
Lacosamide 200 mg/1 · Tablet, Film Coated · Oral
Product NDC51991-351
Product details
- Brand name
- Lacosamide
- Generic name
- Lacosamide
- Labeler
- Breckenridge Pharmaceutical, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA204921
- Marketed since
- March 18, 2022
- Listing expires
- December 31, 2026
Active ingredients
- Lacosamide 200 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 51991-351-05 | 500 TABLET, FILM COATED in 1 BOTTLE (51991-351-05) | Mar 18, 2022 |
| 51991-351-06 | 60 TABLET, FILM COATED in 1 BOTTLE (51991-351-06) | Mar 18, 2022 |
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