Sumatriptan
- Product NDC
- 63629-8134
- 11-digit product format
- 636298134
- Labeler code
- 63629
- Product ID
- 63629-8134_d68f0ce2-d6e0-4901-ba43-f33a43186440
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sumatriptan Succinate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078327
- Marketing category
- ANDA
- Marketing start
- 2009-08-17
- Marketing end
- 0000-00-00
- Substance
- SUMATRIPTAN SUCCINATE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC],Serotonin 1b Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 63629-8134-1 | 63629813401 | 9 TABLET in 1 BOTTLE (63629-8134-1) | 9 tablet | 2019-07-29 | 0000-00-00 | No | No | Current |