Sumatriptan Succinate
- Product NDC
- 16714-040
- 11-digit product format
- 167140040
- Labeler code
- 16714
- Product ID
- 16714-040_26e6a48e-52c7-8fa6-5bd8-69241b5e84c9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sumatriptan Succinate
- Dosage form
- INJECTION
- Route
- SUBCUTANEOUS
- Labeler
- NorthStar Rx LLC
- Application
- ANDA090495
- Marketing category
- ANDA
- Marketing start
- 2021-09-08
- Marketing end
- 0000-00-00
- Substance
- SUMATRIPTAN SUCCINATE
- Active strength
- 6 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 16714-040-02 | 16714004002 | 2 SYRINGE in 1 CARTON (16714-040-02) > .5 mL in 1 SYRINGE (16714-040-01) | 2 syringe | 2021-09-08 | 0000-00-00 | No | No | Current |