NDC 31722-814 – Lacosamide
Lacosamide 150 mg/1 · Tablet, Film Coated · Oral
Product NDC31722-814
Product details
- Brand name
- Lacosamide
- Generic name
- Lacosamide
- Labeler
- Camber Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA204787
- Marketed since
- March 17, 2022
- Listing expires
- December 31, 2027
Active ingredients
- Lacosamide 150 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 31722-814-05 | 500 TABLET, FILM COATED in 1 BOTTLE (31722-814-05) | Mar 17, 2022 |
| 31722-814-18 | 180 TABLET, FILM COATED in 1 BOTTLE (31722-814-18) | Mar 17, 2022 |
| 31722-814-32 | 100 TABLET, FILM COATED in 1 BLISTER PACK (31722-814-32) | Mar 17, 2022 |
| 31722-814-60 | 60 TABLET, FILM COATED in 1 BOTTLE (31722-814-60) | Mar 17, 2022 |
Recalls mentioning this NDC
- D-0626-2026 Jul 1, 2026 · Class II
Presence of a Foreign Tablets: Complaint received, possible mix-up of Selexipag 1000 mcg tablet in a bottle of Lacosamide Tablets USP, 100mg.
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