Rizatriptan Benzoate
- Product NDC
- 72189-512
- 11-digit product format
- 721890512
- Labeler code
- 72189
- Product ID
- 72189-512_2c4e6424-181c-1db8-e063-6294a90a52d9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Rizatriptan Benzoate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA202490
- Marketing category
- ANDA
- Marketing start
- 2023-09-11
- Substance
- RIZATRIPTAN BENZOATE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Serotonin 1b Receptor Agonists [MoA], Serotonin 1d Receptor Agonists [MoA], Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| WR978S7QHH | RIZATRIPTAN BENZOATE | 145202-66-0 | RIZATRIPTAN BENZOATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72189-512-18 | 72189051218 | 18 TABLET in 1 BOTTLE (72189-512-18) | 18 tablet | 2023-09-11 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Rizatriptan Benzoate | Direct_Rx | 2025-01-22 | HUMAN PRESCRIPTION DRUG LABEL | 3 |