Rizatriptan
- Product NDC
- 50090-7747
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Rizatriptan
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA203147
- Marketing category
- ANDA
- Substance
- RIZATRIPTAN BENZOATE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 50090-7747-0 | 3 BLISTER PACK in 1 CARTON (50090-7747-0) / 6 TABLET, FILM COATED in 1 BLISTER PACK | 2025-11-03 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Rizatriptan | A-S Medication Solutions | 2025-11-05 | Human Prescription Drug Label | 1 |