Sumatriptan
- Product NDC
- 0093-2013
- 11-digit product format
- 000932013
- Labeler code
- 0093
- Product ID
- 0093-2013_c70368a4-4b28-4d08-aff9-85f4106834ff
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- sumatriptan succinate
- Dosage form
- INJECTION
- Route
- SUBCUTANEOUS
- Labeler
- Teva Pharmaceuticals USA Inc
- Application
- ANDA078319
- Marketing category
- ANDA
- Marketing start
- 2016-06-01
- Marketing end
- 0000-00-00
- Substance
- SUMATRIPTAN SUCCINATE
- Active strength
- 4 mg/.5mL
- 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
Additional Listing Data#
- Finished product
- No
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SUMATRIPTAN SUCCINATE | 4 mg/.5mL |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0093-2013-12 | 00093201312 | 2 SYRINGE in 1 CARTON (0093-2013-12) > .5 mL in 1 SYRINGE (0093-2013-34) | 2 syringe | 2016-06-01 | 0000-00-00 | No | No | Current |
| 0093-2013-99 | 00093201399 | 2400 SYRINGE in 1 BOX (0093-2013-99) / .5 mL in 1 SYRINGE | 2400 syringe | 24-MAR-22 | | | | Current |