SUMATRIPTAN
- Product NDC
- 0781-6524
- 11-digit product format
- 007816524
- Labeler code
- 0781
- Product ID
- 0781-6524_f9989be0-513c-4c19-a4cf-4069531895ed
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- sumatriptan
- Dosage form
- SPRAY
- Route
- NASAL
- Labeler
- Sandoz Inc
- Application
- NDA020626
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2008-09-11
- Marketing end
- 2022-01-31
- Substance
- SUMATRIPTAN
- Active strength
- 5 mg/100uL
- 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 |
|---|
| 0781-6524-86 | 00781652486 | 6 CONTAINER in 1 BOX (0781-6524-86) > 100 uL in 1 CONTAINER (0781-6524-06) | 6 container | 2008-09-11 | 0000-00-00 | No | No | Current |