NDC 67877-261 – Rizatriptan Benzoate
Rizatriptan Benzoate 5 mg/1 · Tablet · Oral
Product NDC67877-261
Product details
- Brand name
- Rizatriptan Benzoate
- Generic name
- Rizatriptan Benzoate
- Labeler
- Ascend Laboratories, LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA203269
- Marketed since
- June 25, 2012
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin-1b and Serotonin-1d Receptor Agonist
Active ingredients
- Rizatriptan Benzoate 5 mg/1
Uses, dosage, side effects and warnings for Rizatriptan Benzoate →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 67877-261-01 | 100 TABLET in 1 BOTTLE (67877-261-01) | Jun 25, 2012 |
| 67877-261-05 | 500 TABLET in 1 BOTTLE (67877-261-05) | Jun 25, 2012 |
| 67877-261-18 | 3 BLISTER PACK in 1 CARTON (67877-261-18) / 6 TABLET in 1 BLISTER PACK | Jun 25, 2012 |
| 67877-261-25 | 2 BLISTER PACK in 1 CARTON (67877-261-25) / 6 TABLET in 1 BLISTER PACK | Jun 25, 2012 |
| 67877-261-30 | 30 TABLET in 1 BOTTLE (67877-261-30) | Jun 25, 2012 |
Recalls mentioning this NDC
- D-0534-2025 Jul 23, 2025 · Class II
CGMP Deviations: detection of N-nitroso-dimethyl-rizatriptan impurity, above the FDA recommended acceptable intake limit. - D-0533-2025 Jul 23, 2025 · Class II
CGMP Deviations: detection of N-nitroso-dimethyl-rizatriptan impurity, above the FDA recommended acceptable intake limit.
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