sumatriptan succinate
- Product NDC
- 68788-7158
- 11-digit product format
- 687887158
- Labeler code
- 68788
- Product ID
- 68788-7158_f2f10649-6012-48ef-acf7-3fb12e93b5e5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- sumatriptan succinate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA078295
- Marketing category
- ANDA
- Marketing start
- 2018-06-05
- Marketing end
- 0000-00-00
- Substance
- SUMATRIPTAN SUCCINATE
- Active strength
- 50 mg/1
- 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
- 2021-12-31
- 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 |
|---|
| 68788-7158-9 | 68788715809 | 9 BLISTER PACK in 1 CARTON (68788-7158-9) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 9 blister pack | 2018-06-05 | 0000-00-00 | No | No | Current |