sumatriptan
- Product NDC
- 67457-879
- 11-digit product format
- 674570879
- Labeler code
- 67457
- Product ID
- 67457-879_6b35dcf4-1400-48b7-bf5e-f98d6fbe41f7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- sumatriptan
- Dosage form
- INJECTION, SOLUTION
- Route
- SUBCUTANEOUS
- Labeler
- Mylan Institutional LLC
- Application
- ANDA090314
- Marketing category
- ANDA
- Marketing start
- 2018-11-06
- Marketing end
- 2021-05-31
- 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
- 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 |
|---|
| 67457-879-05 | 67457087905 | 2 BLISTER PACK in 1 CARTON (67457-879-05) > 1 SYRINGE in 1 BLISTER PACK (67457-879-00) > .5 mL in 1 SYRINGE | 2 blister pack | 2018-11-06 | 2021-05-31 | No | No | Current |