NDC 68462-714 – Rufinamide
Rufinamide 400 mg/1 · Tablet, Film Coated · Oral
Product NDC68462-714
Product details
- Brand name
- Rufinamide
- Generic name
- Rufinamide
- Labeler
- Glenmark Pharmaceuticals Inc., USA
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA205075
- Marketed since
- May 16, 2016
- Listing expires
- December 31, 2027
Active ingredients
- Rufinamide 400 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 68462-714-05 | 500 TABLET, FILM COATED in 1 BOTTLE (68462-714-05) | May 16, 2016 |
| 68462-714-08 | 120 TABLET, FILM COATED in 1 BOTTLE (68462-714-08) | May 16, 2016 |
Recalls mentioning this NDC
- D-0323-2025 Apr 16, 2025 · Class II
CGMP Deviations
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