Sumatriptan Succinate
- Product NDC
- 70518-3179
- 11-digit product format
- 705183179
- Labeler code
- 70518
- Product ID
- 70518-3179_c8c1b4ca-93c9-221b-e053-2a95a90a3a48
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sumatriptan Succinate
- Dosage form
- INJECTION
- Route
- SUBCUTANEOUS
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA090495
- Marketing category
- ANDA
- Marketing start
- 2021-08-04
- 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
- 2022-12-31
- 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 |
|---|
| 70518-3179-0 | 70518317900 | 2 SYRINGE in 1 CARTON (70518-3179-0) > .5 mL in 1 SYRINGE | 2 syringe | 2021-08-04 | 0000-00-00 | No | No | Current |