Rizatriptan Benzoate
- Product NDC
- 71205-644
- 11-digit product format
- 712050644
- Labeler code
- 71205
- Product ID
- 71205-644_fad5d266-a87f-413a-b644-8ebbe93e7534
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Rizatriptan Benzoate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA202490
- Marketing category
- ANDA
- Marketing start
- 2012-12-31
- Substance
- RIZATRIPTAN BENZOATE
- Active strength
- 10 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 |
|---|
| 71205-644-12 | 71205064412 | 4 BLISTER PACK in 1 CARTON (71205-644-12) / 3 TABLET in 1 BLISTER PACK | 4 blister pack | 2022-03-16 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Rizatriptan Benzoate | Proficient Rx LP | 2022-05-01 | HUMAN PRESCRIPTION DRUG LABEL | 2 |