Rizatriptan Benzoate
- Product NDC
- 71335-1257
- 11-digit product format
- 713351257
- Labeler code
- 71335
- Product ID
- 71335-1257_4885e0c5-4bd3-4e6e-b34b-ee6689432afb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Rizatriptan Benzoate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA207836
- Marketing category
- ANDA
- Marketing start
- 2017-03-07
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-1257-1 | 71335125701 | 30 TABLET in 1 BOTTLE (71335-1257-1) | 30 tablet | 2019-06-27 | 0000-00-00 | No | No | Current |
| 71335-1257-2 | 71335125702 | 18 TABLET in 1 BOTTLE (71335-1257-2) | 18 tablet | 2019-06-27 | 0000-00-00 | No | No | Current |