SUMATRIPTAN SUCCINATE
- Product NDC
- 0781-3174
- 11-digit product format
- 007813174
- Labeler code
- 0781
- Product ID
- 0781-3174_11978034-eb0c-4d7f-ab70-4375b71c1684
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- sumatriptan succinate
- Dosage form
- INJECTION, SOLUTION
- Route
- SUBCUTANEOUS
- Labeler
- Sandoz Inc
- Application
- NDA020080
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2008-09-09
- Marketing end
- 0000-00-00
- Substance
- SUMATRIPTAN SUCCINATE
- Active strength
- 6 mg/.5mL
- 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
- 2021-12-31
- 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 |
|---|
| 0781-3174-14 | 00781317414 | 5 VIAL in 1 CARTON (0781-3174-14) > .5 mL in 1 VIAL (0781-3174-71) | 5 vial | 2008-09-09 | 0000-00-00 | No | No | Current |