NDC 68462-678 – Lacosamide
Lacosamide 50 mg/1 · Tablet, Film Coated · Oral
Product NDC68462-678
Product details
- Brand name
- Lacosamide
- Generic name
- Lacosamide
- Labeler
- Glenmark Pharmaceuticals Inc. USA
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA205006
- Marketed since
- March 18, 2022
- Listing expires
- December 31, 2026
Active ingredients
- Lacosamide 50 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 68462-678-10 | 1000 TABLET, FILM COATED in 1 BOTTLE (68462-678-10) | Mar 18, 2022 |
| 68462-678-30 | 30 TABLET, FILM COATED in 1 BOTTLE (68462-678-30) | Mar 18, 2022 |
| 68462-678-60 | 60 TABLET, FILM COATED in 1 BOTTLE (68462-678-60) | Mar 18, 2022 |
Recalls mentioning this NDC
- D-0330-2025 Apr 16, 2025 · Class II
CGMP Deviations - D-0321-2025 Apr 16, 2025 · Class II
CGMP Deviations - D-0337-2025 Apr 16, 2025 · Class II
CGMP Deviations - D-0343-2025 Apr 16, 2025 · Class II
CGMP Deviations
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