NDC 47335-922 – Lacosamide
Lacosamide 100 mg/1 · Tablet, Film Coated · Oral
Product NDC47335-922
Product details
- Brand name
- Lacosamide
- Generic name
- Lacosamide
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA205031
- Marketed since
- March 19, 2022
- Listing expires
- December 31, 2026
Active ingredients
- Lacosamide 100 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 47335-922-18 | 1000 TABLET, FILM COATED in 1 BOTTLE (47335-922-18) | Mar 19, 2022 |
| 47335-922-82 | 180 TABLET, FILM COATED in 1 BOTTLE (47335-922-82) | Mar 19, 2022 |
| 47335-922-86 | 60 TABLET, FILM COATED in 1 BOTTLE (47335-922-86) | Mar 19, 2022 |
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