Rizatriptan Benzoate
- Product NDC
- 70518-0509
- 11-digit product format
- 705180509
- Labeler code
- 70518
- Product ID
- 70518-0509_e1e13499-76d5-340f-e053-2a95a90acdb6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- rizatriptan benzoate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA201993
- Marketing category
- ANDA
- Marketing start
- 2017-05-09
- Marketing end
- 0000-00-00
- 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
- 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 |
|---|
| 70518-0509-0 | 70518050900 | 10 TABLET in 1 BOTTLE, PLASTIC (70518-0509-0) | 10 tablet | 2017-05-09 | 0000-00-00 | No | No | Current |
| 70518-0509-1 | 70518050901 | 6 TABLET in 1 BOTTLE, PLASTIC (70518-0509-1) | 6 tablet | 2020-09-14 | 0000-00-00 | No | No | Current |
| 70518-0509-2 | 70518050902 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-0509-2) | 90 tablet | 2021-02-16 | 0000-00-00 | No | No | Current |