IMITREX
- Product NDC
- 0173-0523
- 11-digit product format
- 001730523
- Labeler code
- 0173
- Product ID
- 0173-0523_1a2c2653-17a8-430b-b9c9-aa3acfe70bed
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- sumatriptan
- Dosage form
- SPRAY
- Route
- NASAL
- Labeler
- GlaxoSmithKline LLC
- Application
- NDA020626
- Marketing category
- NDA
- Marketing start
- 1997-09-18
- Marketing end
- 0000-00-00
- Substance
- SUMATRIPTAN
- Active strength
- 20 mg/1
- 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
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0173-0523 | IMITREX (SUMATRIPTAN) SPRAY [GLAXOSMITHKLINE LLC] | 22 | Legacy NDC | 20240328_cc11b09d-e6cc-4cf8-1495-5ac64d5aae5f.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0173-0523-00 | 00173052300 | 6 CONTAINER in 1 BOX (0173-0523-00) > 1 SPRAY in 1 CONTAINER | 6 container | 1997-09-18 | 0000-00-00 | No | No | Current |