SUMATRIPTAN SUCCINATE
- Product NDC
- 0781-3169
- 11-digit product format
- 007813169
- Labeler code
- 0781
- Product ID
- 0781-3169_14af8714-8244-4245-82be-77d1b2d3cf73
- 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
- 2012-01-12
- Marketing end
- 2021-09-30
- Substance
- SUMATRIPTAN SUCCINATE
- Active strength
- 4 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
- 0000-00-00
- 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 |
|---|
| 0781-3169-07 | 00781316907 | 1 PACKAGE in 1 CARTON (0781-3169-07) > 2 SYRINGE in 1 PACKAGE > .5 mL in 1 SYRINGE | 1 package | 2012-01-12 | 0000-00-00 | No | No | Current |